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 |