Atlas FDA

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

M.P. Video, Inc. · Predicate Candidate Screening

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

61 daysmedian FDA review time
97 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K951386COMBINATION CAMERA/LIGHT SOURCEM.P. Video, Inc.1995-06-30950
K943342MEDICAM XENON LIGHT SOURCEM.P. Video, Inc.1994-10-17970
K942358AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERAM.P. Video, Inc.1994-08-08830
K941773MEDICAM 900 REMOTEM.P. Video, Inc.1994-07-18980
K941693MEDICAM ENDOCOUPLER AND BEAMSPLITTERM.P. Video, Inc.1994-06-27820
K893828ML-800 AUTOELECTRONIC LIGHT SOURCEM.P. Video, Inc.1989-07-24610
K882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERASM.P. Video, Inc.1988-07-26130
K871595SURGICAL CAMERA ACCESSORIESM.P. Video, Inc.1987-05-07130
K871057MC-SERIES SURGICAL CAMERASM.P. Video, Inc.1987-04-03170
K871056MEDICAM S-4 SURGICAL CAMERAM.P. Video, Inc.1987-03-31140
K820829MEDICAMM.P. Video, Inc.1982-05-03390

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