K212186 is an FDA 510(k) clearance for the Philips Radiology Smart Assistant. This device is classified as a System, X-ray, Stationary (Class II - Special Controls, product code KPR).
Submitted by Philips Medical Systems Dmc GmbH (Hamburg, DE). The FDA issued a Cleared decision on December 13, 2021, 153 days after receiving the submission on July 13, 2021.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K212186 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 13, 2021 |
| Decision Date | December 13, 2021 |
| Days to Decision | 153 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | KPR — System, X-ray, Stationary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |