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

QUICK-CHECK II REAGENT STRIP

K Number: K921825 · Decision Aug 18, 1992
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
26
Review Days
124

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Basic Information

Device Name
QUICK-CHECK II REAGENT STRIP
K Number
K921825
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Solutions, Inc.
Date Received
April 16, 1992
Decision Date
August 18, 1992
Product Code
CGA
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
CGA Glucose Oxidase, Glucose

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Other Clearances by Diagnostic Solutions, Inc.

K Number Device Name
K934892 RELIEF PLUS ONE REAGENT STRIP MODIFICATION
K924398 UNI-CHECK REAGENT STRIP
K800689 REAGENT FOR DETERM. GLUTAMIC-PYRUVIC-
K800681 REAGENTS FOR DETERM. CO2 IN HUMAN SERUM
K800672 SMAC REPLACEMENT REAGENTS/DETERM-URIC-AC
K800674 SMAC REPLACEMENT/TOTAL PROTEIN HUMAN SER
K800687 REAGENT FOR DETERM. GLUCOSE IN H/SERUM
K800679 REAGENTS FOR DETERM. ALKALINE PHOSPHATAS
K800685 REAGENT FOR DETERM. CREATININE IN H/SERU
K800692 REAGENT FOR DETERM. POTASSIUM/IN HUMAN
Search all 26 clearances from Diagnostic Solutions, Inc. →