K973219 is an FDA 510(k) clearance for the AMBER DU. This device is classified as a System, X-ray, Stationary (Class II - Special Controls, product code KPR).
Submitted by Oldelft Corp. of America (Columbia, US). The FDA issued a Cleared decision on October 8, 1997, 42 days after receiving the submission on August 27, 1997.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K973219 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 27, 1997 |
| Decision Date | October 08, 1997 |
| Days to Decision | 42 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | KPR — System, X-ray, Stationary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |