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

EBNA ENZYME IMMUNOASSAY KIT

K Number: K951822 · Decision Feb 15, 1996
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
26
Applicant Total
8
Review Days
301

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Basic Information

Device Name
EBNA ENZYME IMMUNOASSAY KIT
K Number
K951822
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3235
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Granbio, Inc.
Date Received
April 20, 1995
Decision Date
February 15, 1996
Product Code
LLM
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
LLM Test, Antigen, Nuclear, Epstein-Barr Virus

Similar 510(k) Clearances

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

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Other Clearances by Granbio, Inc.

K Number Device Name
K934774 UNKNOWN
K901156 EIA FOR IGG ANTIBODY TO EBV VCA IN HUMAN SERUM
K901840 (EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM
K881617 INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY
K871298 EBNA ACIF ASSAY KIT
K864347 INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCA
K864604 EBV VCA IGM ANTIBODY ASSAY KIT