Acumedia Manufacturers, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acumedia Manufacturers, Inc. - FDA 510(k) Cleared Devices
177
Total
177
Cleared
0
Denied
Acumedia Manufacturers, Inc. has 177 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 177 cleared submissions from 1981 to 1988.
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 - Acumedia Manufacturers, Inc.
177 devices
Cleared
Apr 18, 1988
DNASE TEST AGAR
Microbiology
10d
Cleared
Apr 18, 1988
DEXTROSE AGAR
Microbiology
10d
Cleared
Apr 18, 1988
DEXTROSE TRYPTONE BROTH
Microbiology
10d
Cleared
Apr 18, 1988
DERMATOPHYTE TEST MEDIUM
Microbiology
10d
Cleared
Apr 18, 1988
COOKED MEAT MEDIUM
Microbiology
10d
Cleared
Apr 18, 1988
CHAPMAN STONE MEDIUM
Microbiology
10d
Cleared
Apr 18, 1988
CASMAN MEDIUM BASE
Microbiology
10d
Cleared
Apr 18, 1988
CASEIN PEPTONE, LOW VITAMIN
Microbiology
10d
Cleared
Apr 18, 1988
CARY AND BLAIR TRANSPORT MEDIUM
Microbiology
10d
Cleared
Apr 18, 1988
BRILLIANT GREEN AGAR W/SULFADIAZINE
Microbiology
10d
Cleared
Apr 18, 1988
BLOOD AGAR BASE, IMPROVED
Microbiology
10d
Cleared
Apr 18, 1988
BLOOD AGAR BASE W/LOW PH
Microbiology
10d
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