FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DIASCAN CONTROL

K Number: K853553 · Decision Sep 16, 1985
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
22
Review Days
21

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Basic Information

Device Name
DIASCAN CONTROL
K Number
K853553
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Home Diagnostics, Inc.
Date Received
August 26, 1985
Decision Date
September 16, 1985
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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Other Clearances by Home Diagnostics, Inc.

K Number Device Name
K090495 TRUEBALANCE BLOOD GLUCOSE SYSTEM
K080641 TRUERESULT BLOOD GLUCOSE SYSTEM E4H01-81
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. →