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

RUBELLA IGM

K Number: K921573 · Decision Aug 27, 1992
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
14
Review Days
147

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Basic Information

Device Name
RUBELLA IGM
K Number
K921573
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clark Laboratories, Inc.
Date Received
April 2, 1992
Decision Date
August 27, 1992
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LFX), ordered by most recent decision date.

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Other Clearances by Clark Laboratories, Inc.

K Number Device Name
K980912 VCA IGG ELISA TEST SYSTEM
K980596 VCA IGM ELISA TEST SYSTEM
K980598 EBNA-1 IGM ELISA TEST SYSTEM
K973123 EA-D IGG ELISA TEST SYSTEM
K931543 ENCORE ENA COMBINED EIA
K925826 ENCORE THYROGLOBULIN IGE, IGA AND IGM EIA
K923537 ENCORE DS-DNA
K921870 ENCORE SM/RNP
K921572 ENCORE SM
K922340 ENCORE SS-B
Search all 14 clearances from Clark Laboratories, Inc. →