K063781 is an FDA 510(k) clearance for the PHILIPS XD-S DIRECT RADIOGRAPHY WORKSTATION/PACKAGE. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by Philips Medical Systems North America Co. (Bothell, US). The FDA issued a Cleared decision on January 5, 2007, 15 days after receiving the submission on December 21, 2006.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K063781 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 21, 2006 |
| Decision Date | January 05, 2007 |
| Days to Decision | 15 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LLZ — System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |