The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Poly Per-q-cath Picc Catheter,model 3236100 And Poly Per-q-cath Midline Catheter, Model 3134135.
| Device ID | K001901 |
| 510k Number | K001901 |
| Device Name: | POLY PER-Q-CATH PICC CATHETER,MODEL 3236100 AND POLY PER-Q-CATH MIDLINE CATHETER, MODEL 3134135 |
| 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 | Michaela Rivkowich |
| Correspondent | Michaela Rivkowich 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-06-22 |
| Decision Date | 2000-09-19 |