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

ENCORE DS-DNA

K Number: K923537 · Decision Dec 23, 1992
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
28
Applicant Total
14
Review Days
160

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Basic Information

Device Name
ENCORE DS-DNA
K Number
K923537
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clark Laboratories, Inc.
Date Received
July 16, 1992
Decision Date
December 23, 1992
Product Code
LRM
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
LRM Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control

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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
K921870 ENCORE SM/RNP
K921572 ENCORE SM
K922340 ENCORE SS-B
K922157 ENCORE SS-A
Search all 14 clearances from Clark Laboratories, Inc. →