The following data is part of a premarket notification filed by Vnus Medical Technologies, Inc. with the FDA for Vnus Closurefast Catheter, Models Cf7-7-60 And Cf7-7-100.
| Device ID | K061373 |
| 510k Number | K061373 |
| Device Name: | VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | VNUS MEDICAL TECHNOLOGIES, INC. 5799 FONTANOSO WAY San Jose, CA 95138 |
| Contact | Carelle L Karimimanesh |
| Correspondent | Carelle L Karimimanesh VNUS MEDICAL TECHNOLOGIES, INC. 5799 FONTANOSO WAY San Jose, CA 95138 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-05-17 |
| Decision Date | 2006-08-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00643169862982 | K061373 | 000 |
| 00643169862975 | K061373 | 000 |
| 00643169862968 | K061373 | 000 |
| 00643169862951 | K061373 | 000 |
| 00763000022273 | K061373 | 000 |
| 00763000702281 | K061373 | 000 |
| 00763000702274 | K061373 | 000 |