The following data is part of a premarket notification filed by Oktas with the FDA for Vista Mini Camera System.
| Device ID | K970369 |
| 510k Number | K970369 |
| Device Name: | VISTA MINI CAMERA SYSTEM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | OKTAS 134 FLANDERS RD. Westborough, MA 01581 |
| Contact | Martin Newman |
| Correspondent | Martin Newman OKTAS 134 FLANDERS RD. Westborough, MA 01581 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-31 |
| Decision Date | 1997-04-14 |
| Summary: | summary |