K942304 is an FDA 510(k) clearance for the MICROFLEX. This device is classified as a Microscope, Surgical, General & Plastic Surgery (Class I - General Controls, product code FSO).
Submitted by Moeller Microsurgical, Inc. (Waldwick, US). The FDA issued a Cleared decision on June 13, 1994, 31 days after receiving the submission on May 13, 1994.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4700.
| 510(k) Number | K942304 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 13, 1994 |
| Decision Date | June 13, 1994 |
| Days to Decision | 31 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FSO — Microscope, Surgical, General & Plastic Surgery |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4700 |