K841723 is an FDA 510(k) clearance for the ADLER CUSTOM PROCEDURE PACKS..
Submitted by Adler Instrument Co. (Mchenry, US). The FDA issued a Cleared decision on August 1, 1984, 98 days after receiving the submission on April 25, 1984.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K841723 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 25, 1984 |
| Decision Date | August 01, 1984 |
| Days to Decision | 98 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |