The following data is part of a premarket notification filed by Antibodies Inc. with the FDA for Amikacin Ria Kit.
Device ID | K802877 |
510k Number | K802877 |
Device Name: | AMIKACIN RIA KIT |
Classification | Radioimmunoassay, Amikacin |
Applicant | ANTIBODIES INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KLQ |
CFR Regulation Number | 862.3035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-11-17 |
Decision Date | 1980-12-19 |