K944552 is an FDA 510(k) clearance for the PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP. This device is classified as a Clip, Implantable (Class II - Special Controls, product code FZP).
Submitted by Pilling Weck, Inc. (Research Triangle Park, US). The FDA issued a Cleared decision on November 7, 1994, 52 days after receiving the submission on September 16, 1994.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4300.
| 510(k) Number | K944552 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 16, 1994 |
| Decision Date | November 07, 1994 |
| Days to Decision | 52 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | FZP — Clip, Implantable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4300 |