The following data is part of a premarket notification filed by Oscor Inc. with the FDA for Introducer Sets, Models Adelante And Adelante-s.
| Device ID | K073100 | 
| 510k Number | K073100 | 
| Device Name: | INTRODUCER SETS, MODELS ADELANTE AND ADELANTE-S | 
| 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 | 2007-11-02 | 
| Decision Date | 2007-11-30 |