M.A. Bioproducts is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
M.A. Bioproducts - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
M.A. Bioproducts has 12 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1980 to 1983.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - M.A. Bioproducts
12 devices
Cleared
Jul 26, 1983
HERPELISA KIT
Microbiology
306d
Cleared
May 25, 1983
MYCOPLASMELISA TEST KIT
Microbiology
159d
Cleared
May 13, 1983
MUMPSELISA TEST KIT
Microbiology
123d
Cleared
May 09, 1983
CYTOMEGELISA STAT
Chemistry
70d
Cleared
May 05, 1983
VARICELISA TEST KIT
Microbiology
139d
Cleared
Aug 03, 1982
CHLAMYDELISA TEST KIT
Microbiology
32d
Cleared
Jul 30, 1982
MEASELISA TEST KIT
Immunology
45d
Cleared
Jan 26, 1982
TOXOELISA TEST KIT
Microbiology
78d
Cleared
Oct 23, 1981
CELL CULTURE REAGENTS
Microbiology
51d
Cleared
Sep 23, 1981
CYTOMEGELISA TEST KIT
Microbiology
58d
Cleared
Dec 18, 1980
RUBELISA IGM TEST KIT
Microbiology
64d
Cleared
Jul 14, 1980
DIGOXIN EIA KIT
Toxicology
18d