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

MICROMEDIC FERRITIN IRMA KIT

K Number: K883746 · Decision Oct 27, 1988
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
4
Review Days
56

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Basic Information

Device Name
MICROMEDIC FERRITIN IRMA KIT
K Number
K883746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Icn Micromedic Systems
Date Received
September 1, 1988
Decision Date
October 27, 1988
Product Code
DBF
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
DBF Ferritin, Antigen, Antiserum, Control

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Other Clearances by Icn Micromedic Systems

K Number Device Name
K884269 SAMPLE IDENTIFICATION STATION MODEL 38010
K880674 MICROMEDIC CRACKPOT RIA KIT
K881102 MICROMEDIC MORPHINE RIA KIT