Granite Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Granite Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INHIBITORY MOLD AGAR PLATE, BRAIN HEART INFUSION AGAR W/5% SHEEP BLOOD, CHLORA, STREPTOCOCCUS ID TRIPLATE SYSTEM
47
Total
47
Cleared
0
Denied
Granite Diagnostics, Inc. has 47 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 47 cleared submissions from 1977 to 1985.
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 - Granite Diagnostics, Inc.
47 devices
Cleared
Mar 29, 1985
INHIBITORY MOLD AGAR PLATE
Microbiology
21d
Cleared
Mar 29, 1985
BRAIN HEART INFUSION AGAR W/5% SHEEP BLOOD, CHLORA
Microbiology
21d
Cleared
Oct 28, 1983
STREPTOCOCCUS ID TRIPLATE SYSTEM
Microbiology
38d
Cleared
Sep 01, 1983
TCBS AGAR
Microbiology
45d
Cleared
May 16, 1983
STREPTOCOCUS ID PLATE
Microbiology
21d
Cleared
Mar 07, 1983
DIPCHEX DIP-SLIDE CULTURE SYS
Microbiology
41d
Cleared
Feb 28, 1983
CAMPY BLOOD AGAR PLATE
Microbiology
34d
Cleared
Dec 03, 1982
LAKED BLOOD AGAR W/PAROMOMYCIN & VANCOM
Pathology
42d
Cleared
Dec 03, 1982
SMITH'S MEDIUM
Microbiology
39d
Cleared
Dec 03, 1982
SCHAEDLER AGARS
Microbiology
32d
Cleared
Nov 17, 1982
STREP SELECTIVE AGAR
Microbiology
36d
Cleared
Nov 16, 1982
CORN MEAL AGAR W/POLYSORBATE 80
Microbiology
35d
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