The following data is part of a premarket notification filed by Orange Medical Instruments, Inc. with the FDA for Click-count U100 Insulin Syringe.
Device ID | K833706 |
510k Number | K833706 |
Device Name: | CLICK-COUNT U100 INSULIN SYRINGE |
Classification | Syringe, Piston |
Applicant | ORANGE MEDICAL INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FMF |
CFR Regulation Number | 880.5860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-10-18 |
Decision Date | 1984-04-05 |