Microanalytic Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microanalytic Research, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Microanalytic Research, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1980 to 1986. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Microanalytic Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microanalytic Research, Inc.
8 devices
Cleared
May 29, 1986
TRYPSIN RIA KIT
Chemistry
66d
Cleared
Apr 14, 1982
MR1 LUTROPIN RIA KIT
Chemistry
27d
Cleared
Apr 06, 1982
MR1 FOLLITROPIN RIA KIT
Chemistry
19d
Cleared
Dec 29, 1981
MRI TOBRAMYCIN RIA KIT
Microbiology
14d
Cleared
Sep 08, 1981
MRI GENTAMICIN RIA KIT
Microbiology
19d
Cleared
Jul 10, 1981
MRI PROLACTIN RIA KIT
Immunology
94d
Cleared
Jan 21, 1981
IMMUNOREACTIVE ESTRIOL RIA KIT
Chemistry
79d
Cleared
Aug 13, 1980
MRI HCG-BETA RIA KIT CAT. #MR-10100
Immunology
48d