K001961 is an FDA 510(k) clearance for the STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE. This device is classified as a Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (Class II - Special Controls, product code DWF).
Submitted by Stoeckert Instrumente (Arvada, US). The FDA issued a Cleared decision on January 25, 2001, 212 days after receiving the submission on June 27, 2000.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4210.
| 510(k) Number | K001961 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 27, 2000 |
| Decision Date | January 25, 2001 |
| Days to Decision | 212 days |
| Submission Type | Abbreviated |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DWF — Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4210 |