K896331 is an FDA 510(k) clearance for the V2465P X-RAY IMAGE INTENSIFIER. This device is classified as a System, X-ray, Fluoroscopic, Image-intensified (Class II - Special Controls, product code JAA).
Submitted by Hamamatsu Photonics K.K. (Bridgewater, US). The FDA issued a Cleared decision on December 22, 1989, 50 days after receiving the submission on November 2, 1989.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1650.
| 510(k) Number | K896331 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 02, 1989 |
| Decision Date | December 22, 1989 |
| Days to Decision | 50 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | - |
| Product Code | JAA - System, X-ray, Fluoroscopic, Image-intensified |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1650 |