Atlas FDA

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

Micor, Inc. — Predicate Candidate Screening

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

107 daysmedian FDA review time
207 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K031600CONDUCTION CATHETERMicor, Inc.2003-08-13840
K003966WUNDCATH CONDUCTION CATHETERMicor, Inc.2001-07-172070
K001717MICOR CONDUCTION CATHETERMicor, Inc.2000-09-201070
K001940MICOR ANESTHESIA CONDUCTION KITMicor, Inc.2000-08-11460
K991879SPRING-WOUND EPIDURAL CATHETERMicor, Inc.1999-10-281480
K861008PERCUTANEOUS CATHETERSMicor, Inc.1986-04-29420
K860339PERCUTANEOUS CATHETERSMicor, Inc.1986-03-31610
K854018ANGIOGRAPHY CATHETERSMicor, Inc.1986-01-161080

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