The following data is part of a premarket notification filed by Universal Medical Instrument Corp. with the FDA for Umi Curved Chemonucleolysis Needle.
Device ID | K842012 |
510k Number | K842012 |
Device Name: | UMI CURVED CHEMONUCLEOLYSIS NEEDLE |
Classification | Needle, Hypodermic, Single Lumen |
Applicant | UNIVERSAL MEDICAL INSTRUMENT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FMI |
CFR Regulation Number | 880.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-05-17 |
Decision Date | 1984-07-06 |