The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for 7f Sherpa Nx Guide Catheter.
| Device ID | K051846 | 
| 510k Number | K051846 | 
| Device Name: | 7F SHERPA NX GUIDE CATHETER | 
| Classification | Catheter, Percutaneous | 
| Applicant | MEDTRONIC VASCULAR 37A CHERRY HILL DR. Danvers, MA 01923 | 
| Contact | Fred L Boucher | 
| Correspondent | Fred L Boucher MEDTRONIC VASCULAR 37A CHERRY HILL DR. Danvers, MA 01923 | 
| Product Code | DQY | 
| CFR Regulation Number | 870.1250 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2005-07-07 | 
| Decision Date | 2005-08-05 | 
| Summary: | summary |