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

QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL)

K Number: K852418 · Decision Jul 15, 1985
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
5
Review Days
38

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Basic Information

Device Name
QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL)
K Number
K852418
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amf Biological and Diagnostics Co.
Date Received
June 7, 1985
Decision Date
July 15, 1985
Product Code
JJY
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJY Multi-Analyte Controls, All Kinds (Assayed)

Similar 510(k) Clearances

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Other Clearances by Amf Biological and Diagnostics Co.

K Number Device Name
K821931 ZETA-CORT
K821553 ZETAPHASE T3 UPTAKE DIAGNOSTIC KIT
K821554 ZETAPHASE T4 RADIOIMMUNOASSAY DIAG. KIT
K812329 ZETA-SERA D