Sclavo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sclavo, Inc. - FDA 510(k) Cleared Devices
82
Total
82
Cleared
0
Denied
Sclavo, Inc. has 82 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 82 cleared submissions from 1977 to 1992.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sclavo, Inc.
82 devices
Cleared
Mar 04, 1992
ELISA CMV IGM
Microbiology
133d
Cleared
Jan 23, 1992
ELISA TOXO IGM
Microbiology
87d
Cleared
Dec 27, 1991
ELISA RUBELLA IGM
Microbiology
85d
Cleared
Dec 27, 1989
NORMAL AND ABNORMAL CONTROL SERA
Chemistry
77d
Cleared
Nov 14, 1989
TOTAL BILIRUBIN L.F.
Chemistry
46d
Cleared
Oct 30, 1989
CREATININE 340 (ENZYMATIC)
Chemistry
27d
Cleared
Jan 27, 1989
ATYPICAL CHOLINESTERASE
Chemistry
528d
Cleared
Jan 27, 1989
CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
Chemistry
387d
Cleared
Jan 27, 1989
CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
Chemistry
380d
Cleared
Dec 29, 1988
SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER
Chemistry
97d
Cleared
Dec 14, 1988
TOTAL IRON BINDING CAPACITY TEST
Chemistry
37d
Cleared
Aug 25, 1988
UNIFAST ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST
Hematology
80d
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