Blue Ridge Media Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blue Ridge Media Co. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Blue Ridge Media Co. has 11 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1982 to 1982.
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 - Blue Ridge Media Co.
11 devices
Cleared
Apr 16, 1982
CULTURE MEDIA, SINGLE BIOCHEM. TEST
Microbiology
21d
Cleared
Apr 16, 1982
CULTURE MEDIA, GENERAL NUTRIENT BROTH
Microbiology
21d
Cleared
Apr 16, 1982
CULTURE MEDIA, MULTIPLE BIOCHEMICAL
Microbiology
21d
Cleared
Apr 16, 1982
CULTURE MEDIA, NON-SELECTIVE/DIFFER
Microbiology
21d
Cleared
Apr 16, 1982
CULTURE MEDIA SELECTIVE BROTH
Microbiology
21d
Cleared
Apr 16, 1982
CULTURE MEDIA, SELECTIVE & DIFFERENTIAL
Microbiology
21d
Cleared
Apr 16, 1982
DULTURE MEDIA, SELECTIVE & NON-DIFFER
Microbiology
21d
Cleared
Apr 16, 1982
ANTIMICROBIAL SUSCEP. TEST, MUELLER
Microbiology
21d
Cleared
Apr 16, 1982
ISOLATION OF PATHOGENIC NEISSERIA
Microbiology
21d
Cleared
Apr 16, 1982
BLUE RIDGE SHEEP BLOOD
Microbiology
21d
Cleared
Apr 16, 1982
BLUE RIDGE RABBIT BLOOD
Microbiology
21d