K933159 is an FDA 510(k) clearance for the XYZ PADS, a Gauze/sponge, Internal, submitted by Aso Corp. (Sarasota, US). The FDA issued a Cleared decision on December 13, 1993, 167 days after receiving the submission on June 29, 1993. This device falls under the General & Plastic Surgery review panel.
| 510(k) Number | K933159 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 29, 1993 |
| Decision Date | December 13, 1993 |
| Days to Decision | 167 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | EFQ — Gauze/sponge, Internal |
| Device Class | — |