The following data is part of a premarket notification filed by Vnus Medical Technologies, Inc. with the FDA for Vnus Closure System.
| Device ID | K982816 |
| 510k Number | K982816 |
| Device Name: | VNUS CLOSURE SYSTEM |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | VNUS MEDICAL TECHNOLOGIES, INC. 238 EAST CARIBBEAN DR. Sunnyvale, CA 94089 |
| Contact | John D'angelo |
| Correspondent | John D'angelo VNUS MEDICAL TECHNOLOGIES, INC. 238 EAST CARIBBEAN DR. Sunnyvale, CA 94089 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-08-11 |
| Decision Date | 1999-03-17 |
| Summary: | summary |