The following data is part of a premarket notification filed by Bard Peripheral Vascular, Inc. with the FDA for Venaflo Ii Vascular Graft.
Device ID | K052282 |
510k Number | K052282 |
Device Name: | VENAFLO II VASCULAR GRAFT |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | BARD PERIPHERAL VASCULAR, INC. 1415 WEST 3RD ST. Tempe, AZ 85281 |
Contact | Glenn Norton |
Correspondent | Glenn Norton BARD PERIPHERAL VASCULAR, INC. 1415 WEST 3RD ST. Tempe, AZ 85281 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-08-22 |
Decision Date | 2005-09-20 |
Summary: | summary |