The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for 4 Fr Single Lumen (sl) Powerpicc Catheter.
| Device ID | K070996 |
| 510k Number | K070996 |
| Device Name: | 4 FR SINGLE LUMEN (SL) POWERPICC CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
| Applicant | C.R. BARD, INC. 5425 WEST AMELIA EARHART DR. Salt Lake City, UT 84116 |
| Contact | Lynn M Kirchoff |
| Correspondent | Lynn M Kirchoff C.R. BARD, INC. 5425 WEST AMELIA EARHART DR. Salt Lake City, UT 84116 |
| Product Code | LJS |
| CFR Regulation Number | 880.5970 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-04-09 |
| Decision Date | 2007-05-08 |
| Summary: | summary |