Atlas FDA

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

Medic, Inc. — Predicate Candidate Screening

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

122 daysmedian FDA review time
253 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K0223951.5T SCANMED PV ARRAYMedic, Inc.2002-08-13210
K951649MODEL #801GE1500 PEDIATRIC ARRAY COILMedic, Inc.1995-06-22730
K942874MODEL #300TO3500 SHOULDER COILMedic, Inc.1994-12-081740
K942873MODEL #700TO3500 NECK/ABDOMINAL COILMedic, Inc.1994-12-021680
K942875MODEL #900TO3500 HEAD/NECK COILMedic, Inc.1994-12-021680
K942355MODEL #310T03500 WRIST COILMedic, Inc.1994-09-161220
K940874MODEL 900GE1500 HEAD/NECK COILMedic, Inc.1994-06-03980
K933295MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNAMedic, Inc.1994-03-172530
K933296MODEL #310GE1500 WRIST COILMedic, Inc.1994-03-172530
K933659MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COILMedic, Inc.1993-11-221180
K933658MODEL 300GE1500 SHOULDER COILMedic, Inc.1993-11-191150
K933297MODEL #510GE1500 LIVER ARRAY COILMedic, Inc.1993-11-021180

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