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

EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEM

K Number: K110435 · Decision Sep 21, 2011
Classifications
1
FEI Numbers
168
Registration Numbers
169
Same Product Code
507
Applicant Total
22
Review Days
218

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Basic Information

Device Name
EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEM
K Number
K110435
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
U. S. Diagnostics, Inc.
Date Received
February 15, 2011
Decision Date
September 21, 2011
Product Code
NBW
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
NBW System, Test, Blood Glucose, Over The Counter

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Other Clearances by U. S. Diagnostics, Inc.

K Number Device Name
K082201 G5 INFINITY BLODO GLUCOSE MONITORING SYSTEM WITH MODEL IGM, 0024A
K061431 EASYGLUCO, MODEL IGM-0002 G2
K051651 G4, MODEL IGM-0004
K870596 PROTHROMBIN TIME TEST
K870685 COAGULATION CONTROL, LEVEL I
K870687 COAGULATION CONTROL, LEVEL III
K870686 COAGULATION CONTROL, LEVEL II
K871283 CYANMETHEMOGLOBIN STANDARD
K870737 U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL
K870738 U.S. DIAGNOSTICS LIQUID CK ISOENZYME CONTROL
Search all 22 clearances from U. S. Diagnostics, Inc. →