The following data is part of a premarket notification filed by Hitachi Medical Systems America, Inc. with the FDA for Hitachi Versiflex.
| Device ID | K991231 |
| 510k Number | K991231 |
| Device Name: | HITACHI VERSIFLEX |
| Classification | System, X-ray, Angiographic |
| Applicant | HITACHI MEDICAL SYSTEMS AMERICA, INC. 12300 TWINBROOK PARKWAY, SUITE 625 Rockville, MD 20852 |
| Contact | T. Whit Athey |
| Correspondent | T. Whit Athey HITACHI MEDICAL SYSTEMS AMERICA, INC. 12300 TWINBROOK PARKWAY, SUITE 625 Rockville, MD 20852 |
| Product Code | IZI |
| CFR Regulation Number | 892.1600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-12 |
| Decision Date | 1999-05-24 |
| Summary: | summary |