K193415 is an FDA 510(k) clearance for the physIQ Heart Rhythm and Respiration Module. This device is classified as a Electrocardiograph (Class II - Special Controls, product code DPS).
Submitted by Physiq, Inc. (Naperville, US). The FDA issued a Cleared decision on June 11, 2020, 185 days after receiving the submission on December 9, 2019.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2340.
| 510(k) Number | K193415 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 09, 2019 |
| Decision Date | June 11, 2020 |
| Days to Decision | 185 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DPS - Electrocardiograph |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2340 |