The following data is part of a premarket notification filed by Amico Lab, Inc. with the FDA for Fitc Antisera To Human Igg.
Device ID | K822676 |
510k Number | K822676 |
Device Name: | FITC ANTISERA TO HUMAN IGG |
Classification | Kappa, Antigen, Antiserum, Control |
Applicant | AMICO LAB, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DFH |
CFR Regulation Number | 866.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-09-03 |
Decision Date | 1982-11-17 |