K173187 is an FDA 510(k) clearance for the MobileDiagnost M50. This device is classified as a System, X-ray, Mobile (Class II - Special Controls, product code IZL).
Submitted by Philips India Limited (Pune, IN). The FDA issued a Cleared decision on November 16, 2017, 45 days after receiving the submission on October 2, 2017.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1720.
| 510(k) Number | K173187 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 02, 2017 |
| Decision Date | November 16, 2017 |
| Days to Decision | 45 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IZL - System, X-ray, Mobile |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1720 |