Sterling Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterling Diagnostics, Inc. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
Sterling Diagnostics, Inc. has 41 FDA 510(k) cleared chemistry devices. Based in Sterling Heights, US.
Historical record: 41 cleared submissions from 1985 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 - Sterling Diagnostics, Inc.
41 devices
Cleared
Jan 21, 1993
MICROPROTEIN REAGENT SET
Chemistry
303d
Cleared
Nov 07, 1991
TRIGLYCERIDES REAGENT SET
Chemistry
21d
Cleared
Oct 31, 1991
SODIUM REAGENT SET
Chemistry
51d
Cleared
Oct 30, 1991
PHOSPHOLIPID REAGENT SET
Chemistry
50d
Cleared
Jul 29, 1986
LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE)
Chemistry
46d
Cleared
Jul 07, 1986
VANILMANDELIC ACID (VMA) REAGENT SET
Chemistry
48d
Cleared
Jul 01, 1986
UREA NITROGEN (GLDH) REAGENT SET (UV)
Chemistry
21d
Cleared
Jul 01, 1986
ALKALINE PHOSPHATASE (PNPP RATE) REAGENT SET
Chemistry
18d
Cleared
Jun 25, 1986
ALT (SGPT) REAGENT SET (UV RATE)
Chemistry
15d
Cleared
Jun 16, 1986
HYDROXYBUTYRATE DEHYDROGENASE (HBD) REAGENT SET
Chemistry
33d
Cleared
May 23, 1986
SALICYLATE REAGENT SET
Toxicology
24d
Cleared
May 23, 1986
SERUM POTASSIUM REAGENT SET
Chemistry
18d
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