Submission Details
| 510(k) Number | K180482 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 23, 2018 |
| Decision Date | November 30, 2018 |
| Days to Decision | 280 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
K180482 is an FDA 510(k) clearance for the ZOLL Propaq M, a Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (Class II — Special Controls, product code MHX), submitted by ZOLL Medical Corporation (Chelsmford, US). The FDA issued a Cleared decision on November 30, 2018, 280 days after receiving the submission on February 23, 2018. This device falls under the Cardiovascular review panel. Regulated under 21 CFR 870.1025.
| 510(k) Number | K180482 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 23, 2018 |
| Decision Date | November 30, 2018 |
| Days to Decision | 280 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | MHX — Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 870.1025 |