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

LYPHOCHEK QUANTITATIVE URINE CONTROL ABNORMAL (2)

K Number: K880495 · Decision Mar 15, 1988
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
60
Applicant Total
319
Review Days
40

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Basic Information

Device Name
LYPHOCHEK QUANTITATIVE URINE CONTROL ABNORMAL (2)
K Number
K880495
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bio-Rad
Date Received
February 4, 1988
Decision Date
March 15, 1988
Product Code
JJW
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
JJW Urinalysis Controls (Assayed And Unassayed)

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