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

MYOGLOBIN ELISA TEST KIT

K Number: K923195 · Decision Nov 6, 1992
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
45
Applicant Total
3
Review Days
129

Basic Information

Device Name
MYOGLOBIN ELISA TEST KIT
K Number
K923195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5680
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
IMMUNO DIAGNOSTIC CENTER, INC.
Date Received
June 30, 1992
Decision Date
November 6, 1992
Product Code
DDR
Advisory Committee
Immunology
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
DDR Myoglobin, Antigen, Antiserum, Control

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K Number Device Name
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