The following data is part of a premarket notification filed by Minxray, Inc. with the FDA for Minxray Hf100h High Frequency Diagnostic X-ray Unit.
| Device ID | K973712 |
| 510k Number | K973712 |
| Device Name: | MINXRAY HF100H HIGH FREQUENCY DIAGNOSTIC X-RAY UNIT |
| Classification | System, X-ray, Mobile |
| Applicant | MINXRAY, INC. 3611 COMMERCIAL AVE. Northbrook, IL 60062 |
| Contact | Keith R Kretchmer |
| Correspondent | Keith R Kretchmer MINXRAY, INC. 3611 COMMERCIAL AVE. Northbrook, IL 60062 |
| Product Code | IZL |
| CFR Regulation Number | 892.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-09-29 |
| Decision Date | 1997-12-12 |
| Summary: | summary |