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 |