GIO · Class I · 21 CFR 864.6150

FDA Product Code GIO: Tube, Collection, Capillary Blood

Leading manufacturers include American Dade, Sherwood Medical Co. and Abco Dealers, Inc..

22
Total
22
Cleared
44d
Avg days
1977
Since

FDA 510(k) Cleared Tube, Collection, Capillary Blood Devices (Product Code GIO)

22 devices
1–22 of 22
Cleared Oct 27, 1994
MONOJECT SAMPLETTE SEPARATOR TUBE
K941291
Sherwood Medical Co.
Chemistry · 224d
Cleared Jan 12, 1988
MONOJECT SAMPLETTE AMBER CAPILLARY SERUM SEPARATOR
K875061
Sherwood Medical Co.
Hematology · 34d
Cleared Mar 25, 1985
CORNING BLOOD COLLECTION CAPILLARY TUBES
K850806
Corning Medical & Scientific
Hematology · 26d
Cleared Nov 13, 1984
MICRO HEMATOCRIT CAPILLARY TUBES
K843892
Abco Dealers, Inc.
Hematology · 41d
Cleared Aug 31, 1983
MONOJET SAMPLETTE ADAPTERS
K832578
Sherwood Medical Co.
Hematology · 29d
Cleared Nov 06, 1981
S/P SURE-CAP
K812921
American Dade
Hematology · 18d
Cleared Nov 06, 1981
S/P SURE-CAP C
K812922
American Dade
Hematology · 18d
Cleared Nov 06, 1981
S/P SURE-CAP N
K812923
American Dade
Hematology · 18d
Cleared Nov 06, 1981
S/P CAPILLARY TUBES, HEPARINIZED (2A)
K812969
American Dade
Hematology · 15d
Cleared Nov 06, 1981
S/P CAPILLARY TUBES, HEPARINIZED (3A)
K812970
American Dade
Hematology · 15d

About Product Code GIO - Regulatory Context