The following data is part of a premarket notification filed by Bmw Medical, Inc. with the FDA for Clampless Valved Catheter.
| Device ID | K962300 |
| 510k Number | K962300 |
| Device Name: | CLAMPLESS VALVED CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
| Applicant | BMW MEDICAL, INC. 5945 SOUTH 350 WEST Murray, UT 84107 |
| Contact | Phil Triolo, Ph.d. |
| Correspondent | Phil Triolo, Ph.d. BMW MEDICAL, INC. 5945 SOUTH 350 WEST Murray, UT 84107 |
| Product Code | LJS |
| CFR Regulation Number | 880.5970 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-13 |
| Decision Date | 1996-09-05 |
| Summary: | summary |