The following data is part of a premarket notification filed by Sorenson Medical, Inc. with the FDA for Ambit Intermittent Ambulatory Infusion Pump.
| Device ID | K033425 |
| 510k Number | K033425 |
| Device Name: | AMBIT INTERMITTENT AMBULATORY INFUSION PUMP |
| Classification | Pump, Infusion |
| Applicant | SORENSON MEDICAL, INC. 1375 WEST 8040 SOUTH West Jordan, UT 84088 -8320 |
| Contact | Douglas Bueschel |
| Correspondent | Douglas Bueschel SORENSON MEDICAL, INC. 1375 WEST 8040 SOUTH West Jordan, UT 84088 -8320 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-10-27 |
| Decision Date | 2003-11-06 |
| Summary: | summary |