The following data is part of a premarket notification filed by Applied Vascular Devices, Inc. with the FDA for Vascular Clamp.
Device ID | K895691 |
510k Number | K895691 |
Device Name: | VASCULAR CLAMP |
Classification | Clamp, Vascular |
Applicant | APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills, CA 92653 |
Contact | Robert P Cooper |
Correspondent | Robert P Cooper APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills, CA 92653 |
Product Code | DXC |
CFR Regulation Number | 870.4450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-09-21 |
Decision Date | 1989-12-13 |