The following data is part of a premarket notification filed by Applied Medical Resources with the FDA for Evs.
Device ID | K963886 |
510k Number | K963886 |
Device Name: | EVS |
Classification | Introducer, Catheter |
Applicant | APPLIED MEDICAL RESOURCES 26051 MERIT CIRCLE BUILDING 104 Laguna Hills, CA 92653 |
Contact | Howard V Rowe |
Correspondent | Howard V Rowe APPLIED MEDICAL RESOURCES 26051 MERIT CIRCLE BUILDING 104 Laguna Hills, CA 92653 |
Product Code | DYB |
CFR Regulation Number | 870.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-26 |
Decision Date | 1997-04-24 |
Summary: | summary |