The following data is part of a premarket notification filed by Medix Medical Electronics (u.s.a.), Inc. with the FDA for Syringe Driver 209.
| Device ID | K813562 |
| 510k Number | K813562 |
| Device Name: | SYRINGE DRIVER 209 |
| Classification | Pump, Infusion |
| Applicant | MEDIX MEDICAL ELECTRONICS (U.S.A.), INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-22 |
| Decision Date | 1982-02-01 |