K923455 is an FDA 510(k) clearance for the HFG 350, 650, 1050. This device is classified as a System, X-ray, Stationary (Class II - Special Controls, product code KPR).
Submitted by Varian Canada, Inc. (Canada L7g 2j4, CA). The FDA issued a Cleared decision on December 28, 1992, 167 days after receiving the submission on July 14, 1992.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K923455 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 14, 1992 |
| Decision Date | December 28, 1992 |
| Days to Decision | 167 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Statement |
| Product Code | KPR — System, X-ray, Stationary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |