Atlas FDA

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

Continental X-Ray Corp. · Predicate Candidate Screening

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

104 daysmedian FDA review time
199 days90th percentile
27clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002Continental X-Ray Corp.1997-09-11730
K962140ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FContinental X-Ray Corp.1996-07-25520
K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6Continental X-Ray Corp.1996-06-27570
K954581ARC SERIESContinental X-Ray Corp.1995-12-21800
K950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270Continental X-Ray Corp.1995-03-31590
K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000Continental X-Ray Corp.1994-08-171050
K942100MODEL TM EP HIGH VOLTAGE GENERATORContinental X-Ray Corp.1994-06-07420
K934686MOLYBDENUM/RHODIUM FILTERSContinental X-Ray Corp.1994-05-262390
K931724ELECTROPHYSIOLOGY (EP) TABLE EP 2000 SERIESContinental X-Ray Corp.1993-06-14820
K925934WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNTContinental X-Ray Corp.1993-03-041040
K921986PATIENT INFORMATION MANAGER (PIM)Continental X-Ray Corp.1992-10-161710
K921875X-RAY CONTROL AND HI-VOLTAGE GENERATORContinental X-Ray Corp.1992-10-151780
K921896TILTING MAGContinental X-Ray Corp.1992-08-031030
K912996MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLEContinental X-Ray Corp.1992-02-032100
K912516CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111Continental X-Ray Corp.1991-11-191660
K911562EDITOR MP 800/HF-850 X-RAY CONTROL AND GENERATORContinental X-Ray Corp.1991-10-241990
K911563INVENTOR RT/EXPLORER TRAUMA UNITContinental X-Ray Corp.1991-10-231980
K912382MILITARY RADIOGRAPHIC FLAT TABLE, CAT # T-9130Continental X-Ray Corp.1991-10-101340
K912515FLOOR MOUNT TUBESTAND-PERFORMER-N 6610.102/S-9110Continental X-Ray Corp.1991-09-191050
K912517FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109Continental X-Ray Corp.1991-09-191050
K912474CLASSIC 4-WAY ELEVATING TABLEContinental X-Ray Corp.1991-09-161050
K913121OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400Continental X-Ray Corp.1991-08-16310
K904114ANATECH X-RAY GENERATORContinental X-Ray Corp.1991-01-031190
K903160LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENSContinental X-Ray Corp.1990-08-08210
K895730X-RAY EQUIPMENT (VARIOUS TYPES)Continental X-Ray Corp.1989-11-06450
K893129CXC FFT-1 NON-TILT STAT RADIO XRAY TAB 4 WA FL TABContinental X-Ray Corp.1989-06-01370
K88158914X14 MULTIFORMAT SPOT FILMER, NO. 6650.400Continental X-Ray Corp.1988-07-18960

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