K960422 is an FDA 510(k) clearance for the PRUITT SAFETY OCCLUSION CATHETER. This device is classified as a Catheter, Intravascular Occluding, Temporary (Class II - Special Controls, product code MJN).
Submitted by Ideas For Medicine, Inc. (Clearwater, US). The FDA issued a Cleared decision on August 7, 1996, 191 days after receiving the submission on January 29, 1996.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4450.
| 510(k) Number | K960422 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 29, 1996 |
| Decision Date | August 07, 1996 |
| Days to Decision | 191 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | MJN — Catheter, Intravascular Occluding, Temporary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4450 |