K820292 is an FDA 510(k) clearance for the EXTRACTOR III..
Submitted by The Anspach Effort, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 2, 1982, 27 days after receiving the submission on February 3, 1982.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K820292 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 03, 1982 |
| Decision Date | March 02, 1982 |
| Days to Decision | 27 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |