The following data is part of a premarket notification filed by Applied Vascular Devices, Inc. with the FDA for Avd Intimax Occlusion Catheter.
Device ID | K910339 |
510k Number | K910339 |
Device Name: | AVD INTIMAX OCCLUSION CATHETER |
Classification | Occluder, Catheter Tip |
Applicant | APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills, CA 92653 |
Contact | Jo Stegwell |
Correspondent | Jo Stegwell APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills, CA 92653 |
Product Code | DQT |
CFR Regulation Number | 870.1370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-01-28 |
Decision Date | 1991-05-29 |