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

Mick Radio-Nuclear Instruments, Inc. — Predicate Candidate Screening

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

80 daysmedian FDA review time
183 days90th percentile
43clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K230155Mick Valencia Applicator SetMick Radio-Nuclear Instruments, Inc.2023-08-302230
K200221CT F/S/D Compatible Applicators (Fletcher), HDR Compatible TMick Radio-Nuclear Instruments, Inc.2020-02-28300
K150979CT/MR Compatible M.A.C. Interstitial GYN TemplateMick Radio-Nuclear Instruments, Inc.2016-05-314140
K142597Vienna SystemMick Radio-Nuclear Instruments, Inc.2015-02-191570
K122840CT HDR TANDEM/RING APPLICATOR WITH RECTAL RETRACTOR MODEL 04Mick Radio-Nuclear Instruments, Inc.2012-12-14880
K063382HDR CT COMPATIBLE SPLIT RING APPLICATORMick Radio-Nuclear Instruments, Inc.2006-12-26480
K063381CT COMPATIBLE F/S/D APPLICATORSMick Radio-Nuclear Instruments, Inc.2006-12-22440
K052351HDR IORT SHIELDED APPLICATORMick Radio-Nuclear Instruments, Inc.2005-10-17490
K051423MICK HDR INTERSTITIAL IMPLANT ACCESSORIESMick Radio-Nuclear Instruments, Inc.2005-07-01300
K040704MODIFICATION TO HENSCHKE HDR CERVIX APPLICATOR AND HILARIS/NMick Radio-Nuclear Instruments, Inc.2004-06-18920
K033828CT COMPATIBLE INTRAUTERINE SLEEVES, CAT #0311, 9406Mick Radio-Nuclear Instruments, Inc.2004-02-02540
K030110CT HDR TANDEM/RING APPLICATOR WITH RECTAL RETRACTORMick Radio-Nuclear Instruments, Inc.2003-04-03801
K020176HDR MIAMI APPLICATORMick Radio-Nuclear Instruments, Inc.2002-04-08800
K011657HDR TANDEM/RING APPLICATOR WITH RECTAL RETRACTORMick Radio-Nuclear Instruments, Inc.2001-08-27902
K001544VAGINAL APPLICATOR SHIELDEDMick Radio-Nuclear Instruments, Inc.2000-11-171830
K993959ISOCENTRIC BEAM CHECKERMick Radio-Nuclear Instruments, Inc.2000-02-14840
K993960PERMA-DOC PHANTOMMick Radio-Nuclear Instruments, Inc.2000-02-14840
K993472SEGMENTED VAGINAL APPLICATORMick Radio-Nuclear Instruments, Inc.2000-01-12900
K993400HDR CONTOUR TP TEMPLATE AND IMPLANT ACCESSORIESMick Radio-Nuclear Instruments, Inc.2000-01-06900
K991107SHADOW TRAYSMick Radio-Nuclear Instruments, Inc.1999-06-29890
K972709TBI STANDMick Radio-Nuclear Instruments, Inc.1997-10-16870
K961601H.A.M. APPLICATORMick Radio-Nuclear Instruments, Inc.1996-12-232420
K913293QUICK SEEDERMick Radio-Nuclear Instruments, Inc.1992-10-134470
K894381GAMMAMED IRIDIUM-192 SOURCEMick Radio-Nuclear Instruments, Inc.1989-11-211270
K891131GAMMAMED 12IMick Radio-Nuclear Instruments, Inc.1989-08-071574
K890485WANG FRONT LOADING APPLICATORMick Radio-Nuclear Instruments, Inc.1989-04-14730
K891377HILARIS-NORI CERVIX APPLICATORMick Radio-Nuclear Instruments, Inc.1989-04-14360
K890341MICK 200-TP AND MICK TP NEEDLEMick Radio-Nuclear Instruments, Inc.1989-03-14501
K871216HILARIS-NORI ENDOMETRIAL APPLICATORMick Radio-Nuclear Instruments, Inc.1987-07-211170
K871217HENSCHKE AFTERLOADING APPLICATORMick Radio-Nuclear Instruments, Inc.1987-07-161120
K871213KUMAR CERVICAL APPLICATORMick Radio-Nuclear Instruments, Inc.1987-07-161120
K871214GRATICULEMick Radio-Nuclear Instruments, Inc.1987-05-08430
K871215DISPOSABLE SHADOW TRAY INSERTSMick Radio-Nuclear Instruments, Inc.1987-04-06110
K850571I-125 IMPLANT GUNMick Radio-Nuclear Instruments, Inc.1985-03-26410
K834308MULTITREAT 48Mick Radio-Nuclear Instruments, Inc.1984-01-10670
K837344BEAM BLOCK SHAPERMick Radio-Nuclear Instruments, Inc.1983-05-09490
K812893SUPERFLABMick Radio-Nuclear Instruments, Inc.1981-12-08540
K811279AFTERLOADING CATHETER SETMick Radio-Nuclear Instruments, Inc.1981-08-181020
K811278EXTENDED TUMOR CALIPERMick Radio-Nuclear Instruments, Inc.1981-06-02250
K811280FLEX-TEMPLATEMick Radio-Nuclear Instruments, Inc.1981-06-02250
K801983SCOTT NEEDLE & SCOTT MICK IMPLANTERMick Radio-Nuclear Instruments, Inc.1980-10-23650
K802032MINI MICK APPLICATORMick Radio-Nuclear Instruments, Inc.1980-10-23620
K781274GAMMA MED IIMick Radio-Nuclear Instruments, Inc.1978-08-10170

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