Submission Details
| 510(k) Number | K161966 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 18, 2016 |
| Decision Date | September 08, 2016 |
| Days to Decision | 52 days |
| Submission Type | Special |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
K161966 is an FDA 510(k) clearance for the PerkinElmer XRpad2 4336 HWC-M Flat Panel Detector, a Solid State X-ray Imager (flat Panel/digital Imager) (Class II — Special Controls, product code MQB), submitted by Perkinelmer, Inc. (Waltham, US). The FDA issued a Cleared decision on September 8, 2016, 52 days after receiving the submission on July 18, 2016. This device falls under the Radiology review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K161966 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 18, 2016 |
| Decision Date | September 08, 2016 |
| Days to Decision | 52 days |
| Submission Type | Special |
| 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 |