K871595 is an FDA 510(k) clearance for the SURGICAL CAMERA ACCESSORIES. This device is classified as a Camera, Surgical And Accessories (Class I - General Controls, product code KQM).
Submitted by M.P. Video, Inc. (North Attleboro, US). The FDA issued a Cleared decision on May 7, 1987, 13 days after receiving the submission on April 24, 1987.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4160.
| 510(k) Number | K871595 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 24, 1987 |
| Decision Date | May 07, 1987 |
| Days to Decision | 13 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | KQM — Camera, Surgical And Accessories |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4160 |