K070557 is an FDA 510(k) clearance for the MP 719, a Dressing, Wound, Drug, submitted by Marine Polymer Technologies, Inc. (Topsfield, US). The FDA issued a Cleared decision on May 23, 2007, 85 days after receiving the submission on February 27, 2007. This device falls under the General & Plastic Surgery review panel.
| 510(k) Number | K070557 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 27, 2007 |
| Decision Date | May 23, 2007 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FRO — Dressing, Wound, Drug |
| Device Class | — |