K122495 is an FDA 510(k) clearance for the PERKINELMER XRD 1622 AP3 MED FLAT PANEL DETECTOR. This device is classified as a Solid State X-ray Imager (flat Panel/digital Imager) (Class II - Special Controls, product code MQB).
Submitted by Perkinelmer, Inc. (Indianapolis, US). The FDA issued a Cleared decision on November 28, 2012, 104 days after receiving the submission on August 16, 2012.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K122495 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 16, 2012 |
| Decision Date | November 28, 2012 |
| Days to Decision | 104 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | MQB - Solid State X-ray Imager (flat Panel/digital Imager) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |