K201907 is an FDA 510(k) clearance for the ClariVein IC. This device is classified as a Catheter, Continuous Flush (Class II - Special Controls, product code KRA).
Submitted by Merit Medical Systems, Inc. (South Jordan, US). The FDA issued a Cleared decision on August 6, 2020, 28 days after receiving the submission on July 9, 2020.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1210.
| 510(k) Number | K201907 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 09, 2020 |
| Decision Date | August 06, 2020 |
| Days to Decision | 28 days |
| Submission Type | Special |
| 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 |