K932323 is an FDA 510(k) clearance for the PERCUTANEOUS INTRODUCER. This device is classified as a Introducer, Catheter (Class II - Special Controls, product code DYB).
Submitted by Medamicus, Inc. (Minneapolis, US). The FDA issued a Cleared decision on November 9, 1993, 182 days after receiving the submission on May 11, 1993.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1340.
| 510(k) Number | K932323 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 11, 1993 |
| Decision Date | November 09, 1993 |
| Days to Decision | 182 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Statement |
| Product Code | DYB — Introducer, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1340 |