The following data is part of a premarket notification filed by Imed Corp. with the FDA for Drop Controller.
| Device ID | K790669 |
| 510k Number | K790669 |
| Device Name: | DROP CONTROLLER |
| Classification | Monitor, Electric For Gravity Flow Infusion Systems |
| Applicant | IMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FLN |
| CFR Regulation Number | 880.2420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-06 |
| Decision Date | 1979-05-14 |