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

UREA NITROGEN (GLDH) REAGENT SET (UV)

K Number: K862210 · Decision Jul 1, 1986
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
41
Review Days
21

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Basic Information

Device Name
UREA NITROGEN (GLDH) REAGENT SET (UV)
K Number
K862210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Sterling Diagnostics, Inc.
Date Received
June 10, 1986
Decision Date
July 1, 1986
Product Code
CDQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

Similar 510(k) Clearances

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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
K862256 ALKALINE PHOSPHATASE (PNPP RATE) REAGENT SET
K862209 ALT (SGPT) REAGENT SET (UV RATE)
K861855 HYDROXYBUTYRATE DEHYDROGENASE (HBD) REAGENT SET
K861713 SERUM POTASSIUM REAGENT SET
Search all 41 clearances from Sterling Diagnostics, Inc. →