K193509 is an FDA 510(k) clearance for the AcQGuide Flex with AcQCross QX, AcQGuide Mini with AcQCross QX. This device is classified as a Introducer, Catheter (Class II - Special Controls, product code DYB).
Submitted by Acutus Medical, Inc. (Carlsbad, US). The FDA issued a Cleared decision on January 17, 2020, 30 days after receiving the submission on December 18, 2019.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1340.
| 510(k) Number | K193509 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 18, 2019 |
| Decision Date | January 17, 2020 |
| Days to Decision | 30 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DYB — Introducer, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1340 |