K231279 is an FDA 510(k) clearance for the Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mm. This device is classified as a Catheter, Continuous Flush (Class II - Special Controls, product code KRA).
Submitted by Ablative Solutions, Inc. (Wakefield, US). The FDA issued a Cleared decision on July 5, 2023, 63 days after receiving the submission on May 3, 2023.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1210.
| 510(k) Number | K231279 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 03, 2023 |
| Decision Date | July 05, 2023 |
| Days to Decision | 63 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | KRA - Catheter, Continuous Flush |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1210 |