FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SALICYLATE REAGENT SET

K Number: K861615 · Decision May 23, 1986
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
28
Applicant Total
41
Review Days
24

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Basic Information

Device Name
SALICYLATE REAGENT SET
K Number
K861615
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3830
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Sterling Diagnostics, Inc.
Date Received
April 29, 1986
Decision Date
May 23, 1986
Product Code
DKJ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DKJ Colorimetry, Salicylate

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Other Clearances by Sterling Diagnostics, Inc.

K Number Device Name
K921412 MICROPROTEIN REAGENT SET
K914609 TRIGLYCERIDES REAGENT SET
K914039 SODIUM REAGENT SET
K914040 PHOSPHOLIPID REAGENT SET
K862255 LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE)
K861962 VANILMANDELIC ACID (VMA) REAGENT SET
K862210 UREA NITROGEN (GLDH) REAGENT SET (UV)
K862256 ALKALINE PHOSPHATASE (PNPP RATE) REAGENT SET
K862209 ALT (SGPT) REAGENT SET (UV RATE)
K861855 HYDROXYBUTYRATE DEHYDROGENASE (HBD) REAGENT SET
Search all 41 clearances from Sterling Diagnostics, Inc. →