The following data is part of a premarket notification filed by Vnus Medical Technologies, Inc. with the FDA for Vnus Closurefast Intravascular Catheter, Models Cf7-7-60-2, Cf7-7-100-2.
Device ID | K082890 |
510k Number | K082890 |
Device Name: | VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | VNUS MEDICAL TECHNOLOGIES, INC. 5799 FONTANOSO WAY San Jose, CA 95138 |
Contact | Elizabeth Trujillo |
Correspondent | Elizabeth Trujillo VNUS MEDICAL TECHNOLOGIES, INC. 5799 FONTANOSO WAY San Jose, CA 95138 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-30 |
Decision Date | 2008-10-15 |
Summary: | summary |