The following data is part of a premarket notification filed by Imed Corp. with the FDA for Gemini Volumetric Infusion Pump/controller.
| Device ID | K933144 |
| 510k Number | K933144 |
| Device Name: | GEMINI VOLUMETRIC INFUSION PUMP/CONTROLLER |
| Classification | Pump, Infusion |
| Applicant | IMED CORP. 9775 BUSINESSPARK AVE. San Diego, CA 92131 -1699 |
| Contact | Ahmad Sajadi |
| Correspondent | Ahmad Sajadi IMED CORP. 9775 BUSINESSPARK AVE. San Diego, CA 92131 -1699 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-28 |
| Decision Date | 1993-10-12 |