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

RUBENOSTIKA(TM) IGM MICROELISA SYSTEM

K Number: K882999 · Decision Jan 31, 1989
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
130
Review Days
197

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Basic Information

Device Name
RUBENOSTIKA(TM) IGM MICROELISA SYSTEM
K Number
K882999
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Organon Teknika Corp.
Date Received
July 18, 1988
Decision Date
January 31, 1989
Product Code
LFX
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

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K993423 BACT/ALERT SA
K993421 BACT/ALERT SN
K993576 BACT/ALERT MP PROCESS BOTTLE
K992432 BACT/ALERT FN
K983762 NUCLISENS CMV PP67
K992401 BACT/ALERT PF
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