K902932 is an FDA 510(k) clearance for the DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL. This device is classified as a Introducer, Catheter (Class II - Special Controls, product code DYB).
Submitted by Datascope Corp. (Oakland, US). The FDA issued a Cleared decision on October 16, 1990, 105 days after receiving the submission on July 3, 1990.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1340.
| 510(k) Number | K902932 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 03, 1990 |
| Decision Date | October 16, 1990 |
| Days to Decision | 105 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | - |
| Product Code | DYB - Introducer, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1340 |