The following data is part of a premarket notification filed by Oscor Inc. with the FDA for Steerable Guiding Sheath, Model Adelante Destino.
Device ID | K120459 |
510k Number | K120459 |
Device Name: | STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO |
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 | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-15 |
Decision Date | 2012-06-29 |
Summary: | summary |