The following data is part of a premarket notification filed by Vnus Medical Technologies, Inc. with the FDA for Modification To Vnus Closure System.
| Device ID | K003092 |
| 510k Number | K003092 |
| Device Name: | MODIFICATION TO VNUS CLOSURE SYSTEM |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | VNUS MEDICAL TECHNOLOGIES, INC. 238 EAST CARIBBEAN DR. Sunnyvale, CA 94089 |
| Contact | Sam Nanavati |
| Correspondent | Sam Nanavati VNUS MEDICAL TECHNOLOGIES, INC. 238 EAST CARIBBEAN DR. Sunnyvale, CA 94089 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-10-03 |
| Decision Date | 2000-12-18 |