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

DIASCAN BLOOD GLUCOSE MONITORING TEST STRIP

K Number: K922137 · Decision Aug 10, 1993
Classifications
1
FEI Numbers
145
Registration Numbers
145
Same Product Code
399
Applicant Total
22
Review Days
475

Basic Information

Device Name
DIASCAN BLOOD GLUCOSE MONITORING TEST STRIP
K Number
K922137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
HOME DIAGNOSTICS, INC.
Date Received
April 22, 1992
Decision Date
August 10, 1993
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 HOME DIAGNOSTICS, INC.

K Number Device Name
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K080710 TRUE2GO BLOOD GLUCOSE SYSTEM, MODEL F4H01-81
K070593 TRACKRECORD DATA MANAGEMENT SOFTWARE
K060793 ELEMENT BLOOD GLUCOSE TEST SYSTEM
K051147 SIDEKICK BLOOD GLUCOSE TEST SYSTEM
K042080 TRACKEASE SMART SYSTEM BLOOD GLUCOSE SYSTEM
K040670 MODIFICATION TO TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER, TEST STRIPS AND GLUCOSE CONTROL
K032657 TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER, BLOOD GLUCOSE TEST STRIPS, AND GLUCOSE CONTROL SOLUTIONS (LOW AND HIGH)
K030703 TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER AND TRUE TRACK SMART SYSTEM BLOOD GLUCOSE TEST STRIPS
Search all 22 clearances from HOME DIAGNOSTICS, INC. →