The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Usci Pro Flo Xt,soft Tip, And Xt Soft Tip Angiographic.
| Device ID | K960056 |
| 510k Number | K960056 |
| Device Name: | USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | C.R. BARD, INC. 1200 TECHNOLOGY PARK DR. Billerica, MA 01821 |
| Contact | Robert T Miragliuolo |
| Correspondent | Robert T Miragliuolo C.R. BARD, INC. 1200 TECHNOLOGY PARK DR. Billerica, MA 01821 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-04 |
| Decision Date | 1996-10-23 |
| Summary: | summary |