Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

FBN — Predicate Candidate Screening

43 FDA 510(k) clearances under this product code; the 50 most recent screened below.

113 daysmedian FDA review time
287 days90th percentile
43clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254153Single-use Video Scope; PB Digital ControllerMirco-Tech (Nanjing) Co., Ltd.2026-04-031020
K253139Disposable Distal CapMirco-Tech (Nanjing) Co., Ltd.2026-03-191750
K251338Cholangioscope Visualization System (Single-use Video CholanScivita Medical Technology Co., Ltd.2026-01-202650
K251170Tangent Single-Use Digital System: Tangent Single-Use DigitaTangent Endoscopy, LLC2025-09-121501
K243535Flexible Video-Choledochoscope (CHV-110J-U); Flexible Video-Shanghai SeeGen Photoelectric Technology Co., Ltd.2025-03-071120
K241444Biliary Pancreaticobiliary Scope SystemShenzhen HugeMed Medical Technical Development Co., Ltd.2025-01-212440
K233752Dragonfly™ Pancreaticobiliary Scope; Dragonfly™ Digital ContCenterPoint Systems, LLC2024-05-021620
K231497Choledochoscope SystemShenzhen HugeMed Medical Technical Development Co., Ltd.2024-03-062870
K231105Flexible Choledochoscope (Model: CS50H-20EU, CS50H-20US)Shanghai AnQing Medical Instrument Co., Ltd.2023-10-171810
K223741Pusen Single Use Flexible Video Cystoscope/Choledochoscope SZhuhai Pusen Medical Technology Co., Ltd.2023-06-221900
K222261Flexible Video-Choledochoscope SystemShanghai SeeGen Photoelectric Technology Co., Ltd.2023-04-202660
K221784Single-use Video Pancreaticobiliary Scope, PB Digital ControMicro-Tech (Nanjing) Co., Ltd.2023-02-162400
K200483SpyGlass Discover Digital Catheter, SpyGlass Discover DigitaBoston Scientific Corporation2020-05-21840
K183636SpyScope DS Access and Delivery Catheter, SpyScope DS II AccBoston Scientific Corporation2019-01-22270
K181439SpyGlass DS and DS II Direct Visualization SystemBoston Scientific Corporation2018-08-23830
K161147EndoCure Model EUR078AEndocure Technologies, Inc.2016-06-07460
K142922SpyGlass DS Direct Visualization SystemBoston Scientific Corporation2015-01-161000
K113120CHF-Y0005Olympus Medical Systems Corp.2012-09-253400
K093507OLYMPUS CHF TYPE Y0003Olympus Medical Systems Corporation2010-03-101171
K081456OLYMPUS CHF TYPE VOlympus Medical Systems Corporation2008-11-061670
K082576XCHF-T160 VIDEOSCOPEOlympus Medical Systems Corporation2008-10-21460
K080586OLYMPUS XCHF TYPE B180Y1Olympus Medical Systems Corporation2008-05-06640
K060269ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEMAcmi Corporation2006-03-31580
K051886OLYMPUS CHOLEDOCHOSCOPE, MODEL XCHF-BP160FOlympus Medical Systems Corporation2005-11-141250
K972926MVM 7.5 FRENCH FLEXIBLE CHOLEDOCHOSCOPEKARL STORZ Endoscopy-America, Inc.1997-10-08610
K971977KSEA 15.5 FR. FLEXIBLE CHOLEDOCHO-FIBERSCOPEKARL STORZ Endoscopy-America, Inc.1997-08-12750
K962172FLEXIBLE MINI-FIBERSCOPESRichard Wolf Medical Instruments Corp.1996-12-021800
K944473XCHF-33 CHOLEDOCHOFIBERSCOPEOlympus America, Inc.1995-11-224390
K953286FCP-9P, FIBER CHOLEDOCHOSCOPEPentax Precision Instrument Corp.1995-11-031131
K951191FCN-15X, FIBER CHOLEDOCHONEPHROSCOPEPentax Precision Instrument Corp.1995-05-30751
K942112KARL STORZ FLEXIBLE CHOLEDOCHOSCOPEKarl Storz Endoscopy1995-02-283020
K933906CHOLEDOCHOSCOPE/ENDOSCOPE MODIFICATIONFujinon, Inc.1994-07-083310
K935834TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPETechnology Marketing Group1994-03-07900
K93138211274 AC FLEXINBLE CHOLEDOCHOSCOPEKARL STORZ Endoscopy-America, Inc.1993-06-18920
K924228OMEGASCOPEOmega Universal Technologies, Ltd.1993-02-261890
K920224DOSCOPE AND ACESSORIESApplied Laparoscopy1992-08-212170
K915681CHOLEDOCHOSCOPEApplied Laparoscopy1992-01-30420
K912120URF-P2 URETERORENOFIBERSCOPE/CHOLEDOCHOFIBERSCOPEOlympus Corp.1991-08-07851
K911480FLEXIBLE CHOLEDOCHOSCOPEUnited States Endoscopy Group, Inc.1991-06-20770
K904799CHF-B20 CHOLEDOCHOSCOPEOlympus Corp.1991-03-271541
K901010FLEXIBLE CHOLEDOCHOSCOPEIntramed Laboratories, Inc.1990-05-22780
K821974PENTAX CHOLEDOCHOFIBERSCOPE, #FCD-15APentax Precision Instrument Corp.1982-08-10390
K771367CHOLEDOCHOSCOPE SYSTEMRichard Wolf Medical Instruments Corp.1977-08-0280

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda