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

VCA IGM ELISA TEST SYSTEM

K Number: K980596 · Decision Jul 22, 1998
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
55
Applicant Total
14
Review Days
155

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Basic Information

Device Name
VCA IGM ELISA TEST SYSTEM
K Number
K980596
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3235
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clark Laboratories, Inc.
Date Received
February 17, 1998
Decision Date
July 22, 1998
Product Code
LSE
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
LSE Epstein-Barr Virus, Other

Similar 510(k) Clearances

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Other Clearances by Clark Laboratories, Inc.

K Number Device Name
K980912 VCA IGG 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
K922157 ENCORE SS-A
Search all 14 clearances from Clark Laboratories, Inc. →