The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Trifusion, Model 0609190/0659350.
| Device ID | K041088 |
| 510k Number | K041088 |
| Device Name: | TRIFUSION, MODEL 0609190/0659350 |
| 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 | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-04-26 |
| Decision Date | 2004-11-01 |
| Summary: | summary |