The following data is part of a premarket notification filed by Immuno Diagnostic Center, Inc. with the FDA for Myoglobin Ria Test Kit.
Device ID | K904038 |
510k Number | K904038 |
Device Name: | MYOGLOBIN RIA TEST KIT |
Classification | Myoglobin, Antigen, Antiserum, Control |
Applicant | IMMUNO DIAGNOSTIC CENTER, INC. 607 S. FRIENDSWOOD SUITE 27 Friendswood, TX 77546 |
Contact | Amal Mukherjee |
Correspondent | Amal Mukherjee IMMUNO DIAGNOSTIC CENTER, INC. 607 S. FRIENDSWOOD SUITE 27 Friendswood, TX 77546 |
Product Code | DDR |
CFR Regulation Number | 866.5680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-09-04 |
Decision Date | 1990-09-24 |