The following data is part of a premarket notification filed by Oscor Inc. with the FDA for Introducer Set, Model Adelante-s Series.
Device ID | K122084 |
510k Number | K122084 |
Device Name: | INTRODUCER SET, MODEL ADELANTE-S SERIES |
Classification | Introducer, Catheter |
Applicant | Oscor Inc. 3816 DE SOTO BLVD. Palm Harbor, FL 34683 |
Contact | Mila Doskocil |
Correspondent | Mila Doskocil Oscor Inc. 3816 DE SOTO BLVD. Palm Harbor, FL 34683 |
Product Code | DYB |
CFR Regulation Number | 870.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-07-16 |
Decision Date | 2012-08-29 |
Summary: | summary |