The following data is part of a premarket notification filed by Vista Medical Technologies, Inc. with the FDA for Vista Illumination System.
| Device ID | K970217 |
| 510k Number | K970217 |
| Device Name: | VISTA ILLUMINATION SYSTEM |
| Classification | Image, Illumination, Fiberoptic, For Endoscope |
| Applicant | VISTA MEDICAL TECHNOLOGIES, INC. 134 FLANDERS RD. Westborough, MA 01581 |
| Contact | Martin Newman |
| Correspondent | Martin Newman VISTA MEDICAL TECHNOLOGIES, INC. 134 FLANDERS RD. Westborough, MA 01581 |
| Product Code | FFS |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-21 |
| Decision Date | 1997-04-02 |
| Summary: | summary |