The following data is part of a premarket notification filed by Immuno Diagnostic Center, Inc. with the FDA for Micro Albumin Eia Test Kit.
Device ID | K912543 |
510k Number | K912543 |
Device Name: | MICRO ALBUMIN EIA TEST KIT |
Classification | Indicator Method, Protein Or Albumin (urinary, Non-quant.) |
Applicant | IMMUNO DIAGNOSTIC CENTER, INC. 9978 MONROE DR., SUITE 303 Dallas, TX 75220 |
Contact | Amal Mukherjee |
Correspondent | Amal Mukherjee IMMUNO DIAGNOSTIC CENTER, INC. 9978 MONROE DR., SUITE 303 Dallas, TX 75220 |
Product Code | JIR |
CFR Regulation Number | 862.1645 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-10 |
Decision Date | 1991-07-19 |