King Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
King Diagnostics, Inc. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
King Diagnostics, Inc. has 41 FDA 510(k) cleared chemistry devices. Based in Walker, US.
Historical record: 41 cleared submissions from 1981 to 1993.
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 - King Diagnostics, Inc.
41 devices
Cleared
Oct 22, 1993
KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT
Chemistry
106d
Cleared
Aug 25, 1993
KING SODIUM/POTASSIUM STANDARD MODIFIED
Chemistry
152d
Cleared
Aug 16, 1993
HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)
Chemistry
129d
Cleared
Jun 15, 1993
KING DIAGNOSTICS CK REAGENT
Chemistry
91d
Cleared
Nov 02, 1992
KING DIAGNOSTICS GLUCOSE (HK) REAGENT
Chemistry
129d
Cleared
Oct 13, 1992
KING DIAGNOSTICS UREA NITROGEN REAGENT
Chemistry
116d
Cleared
Oct 05, 1992
KING DIAGNOSTICS CHLORIDE REAGENT
Chemistry
110d
Cleared
Sep 30, 1992
KING DIAGNOSTICS MAGNESIUM REAGENT
Chemistry
56d
Cleared
Sep 09, 1992
KING DIAGNOSTICS GAMMA GT REAGENT
Chemistry
76d
Cleared
Sep 09, 1992
KING DIAGNOSTICS CHOLESTEROL REAGENT
Chemistry
75d
Cleared
Aug 18, 1992
KING DIAGNOSTIC TRIGLYCERIDES REAGENT
Chemistry
60d
Cleared
Aug 04, 1992
CALCIUM (AZ III) REAGENT
Chemistry
53d
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