The following data is part of a premarket notification filed by Medtronics Interventional Vascular with the FDA for Medtronic Mustang Super Floppy Guide Wire/floppy Guide Wire/intermediate Guide Wire/standard Guide Wire/extra Support.
| Device ID | K972944 |
| 510k Number | K972944 |
| Device Name: | MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT |
| Classification | Wire, Guide, Catheter |
| Applicant | MEDTRONICS INTERVENTIONAL VASCULAR 9410 CARROLL PARK DR. San Diego, CA 92121 -2256 |
| Contact | Mary De Armond |
| Correspondent | Mary De Armond MEDTRONICS INTERVENTIONAL VASCULAR 9410 CARROLL PARK DR. San Diego, CA 92121 -2256 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-11 |
| Decision Date | 1997-11-03 |
| Summary: | summary |