The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Infusion Set For Powerpicc Solo 2 Catheter.
Device ID | K102405 |
510k Number | K102405 |
Device Name: | INFUSION SET FOR POWERPICC SOLO 2 CATHETER |
Classification | Set, Administration, Intravascular |
Applicant | C.R. BARD, INC. 605 NORTH 5600 WEST Salt Lake City, UT 84116 |
Contact | Lynn M Kirchoff |
Correspondent | Lynn M Kirchoff C.R. BARD, INC. 605 NORTH 5600 WEST Salt Lake City, UT 84116 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-24 |
Decision Date | 2011-07-21 |
Summary: | summary |