Isle Media and Sterile Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isle Media and Sterile Products, Inc. - FDA 510(k) Cleared Devices
93
Total
93
Cleared
0
Denied
Isle Media and Sterile Products, Inc. has 93 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 93 cleared submissions from 1979 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 - Isle Media and Sterile Products, Inc.
93 devices
Cleared
Jul 28, 1983
MODIFIED SOYBEAN CASEIN DIGEST BROTH
Microbiology
66d
Cleared
May 14, 1982
CAMPY-S AGAR
Microbiology
17d
Cleared
Apr 16, 1982
MEDIA FOR IN-VITRO DIAGNOSTIC USE
Microbiology
18d
Cleared
Oct 20, 1981
ANAEROBIC BLOOD AGAR
Microbiology
14d
Cleared
Oct 20, 1981
ANAEROBIC CNA BLOOD AGAR
Microbiology
14d
Cleared
Oct 20, 1981
SCHAEDLER AGARS
Microbiology
14d
Cleared
Oct 20, 1981
MOTILITY GI MEDIUM
Microbiology
14d
Cleared
Apr 24, 1980
CORN MEAL AGAR MEDIA
Microbiology
14d
Cleared
Apr 24, 1980
CHLAMYDOSPORE AGAR
Microbiology
13d
Cleared
Mar 03, 1980
MODIFIED THAYER-MARTIN X AGAR
Microbiology
18d
Cleared
Mar 03, 1980
MARTIN-LEWIS AGAR
Microbiology
18d
Cleared
Feb 13, 1980
STAPHYLOCOCCUS MED. 110
Microbiology
20d
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