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

URISTIK H SERIES REAGENT STRIPS FOR URINALYSIS

K Number: K040703 · Decision Aug 26, 2004
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
10
Applicant Total
1
Review Days
162

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Basic Information

Device Name
URISTIK H SERIES REAGENT STRIPS FOR URINALYSIS
K Number
K040703
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dirui Industrial Co., Ltd.
Date Received
March 17, 2004
Decision Date
August 26, 2004
Product Code
JIO
Advisory Committee
Hematology
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
JIO Blood, Occult, Colorimetric, In Urine

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