K896303 is an FDA 510(k) clearance for the BIOPSY PUNCH. This device is classified as a Punch, Surgical (Class I - General Controls, product code LRY).
Submitted by Premier Medical (Norristown, US). The FDA issued a Cleared decision on February 13, 1990, 106 days after receiving the submission on October 30, 1989.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K896303 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 30, 1989 |
| Decision Date | February 13, 1990 |
| Days to Decision | 106 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | LRY — Punch, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4800 |