The following data is part of a premarket notification filed by Shimadzu Medical Systems with the FDA for Circlexo.3t X-ray Tube Assembly.
| Device ID | K920387 |
| 510k Number | K920387 |
| Device Name: | CIRCLEXO.3T X-RAY TUBE ASSEMBLY |
| Classification | Assembly, Tube Housing, X-ray, Diagnostic |
| Applicant | SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
| Contact | De Mint |
| Correspondent | De Mint SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
| Product Code | ITY |
| CFR Regulation Number | 892.1760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-30 |
| Decision Date | 1992-04-14 |