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

SERATEST DNA DETERMINATION

K Number: K842563 · Decision Oct 25, 1984
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
49
Applicant Total
20
Review Days
115

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Basic Information

Device Name
SERATEST DNA DETERMINATION
K Number
K842563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Seragen Diagnostics, Inc.
Date Received
July 2, 1984
Decision Date
October 25, 1984
Product Code
LKJ
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
LKJ Antinuclear Antibody, Antigen, Control

Similar 510(k) Clearances

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Other Clearances by Seragen Diagnostics, Inc.

K Number Device Name
K872148 VIVID CHLAMYDIA(TM)
K851663 QUICK-COUNT HEMATOLOGY CONTROLS
K852260 QUICK-CHEM CALIBRATION SET
K851520 CK/LD ISOENZYMES CONTROLS(HUMAN)
K851521 LD-1(IMMUNO) SEPARATION SET
K850209 QUICK-LYTE
K844743 SERATEST ENA(RNP/SM) DETERMINATION
K841504 QUICK-COUNT PLUS 2
K840793 CK/MB IMMUNO-ISOENZYME CONTROL SERUM
K840863 SERATEST RF LATEX DETERMINATION
Search all 20 clearances from Seragen Diagnostics, Inc. →