The following data is part of a premarket notification filed by Block Medical, Inc. with the FDA for Verifuse Ambulatory Pump.
| Device ID | K902891 |
| 510k Number | K902891 |
| Device Name: | VERIFUSE AMBULATORY PUMP |
| Classification | Pump, Infusion |
| Applicant | BLOCK MEDICAL, INC. 5957 LANDAU COURT Carlsbad, CA 92008 |
| Contact | Gregory E Sancoff |
| Correspondent | Gregory E Sancoff BLOCK MEDICAL, INC. 5957 LANDAU COURT Carlsbad, CA 92008 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-07-02 |
| Decision Date | 1990-11-21 |