The following data is part of a premarket notification filed by Impra, Inc. with the FDA for Vascular Graft Prosthesis Expanded Micr.
Device ID | K830543 |
510k Number | K830543 |
Device Name: | VASCULAR GRAFT PROSTHESIS EXPANDED MICR |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | IMPRA, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-02-22 |
Decision Date | 1983-07-19 |