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

IMMUNODOT INFECTIOUS MONONUCLEOSIS TEST

K Number: K894975 · Decision Sep 13, 1989
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
58
Applicant Total
23
Review Days
37

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Basic Information

Device Name
IMMUNODOT INFECTIOUS MONONUCLEOSIS TEST
K Number
K894975
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5640
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
General Biometrics, Inc.
Date Received
August 7, 1989
Decision Date
September 13, 1989
Product Code
KTN
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
KTN System, Test, Infectious Mononucleosis

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Other Clearances by General Biometrics, Inc.

K Number Device Name
K924843 IMMUNODOT(R) ENA/DNA AUTOIMMUNITY SCREENING PANEL
K920401 IMMUNOWELL CARDIOLIPIN ANTIBODY (IGM) TEST
K920400 IMMUNOWELL CARDIOLIPIN ANTIBODY (IGG) TEST
K911627 IMMUNODOT BORRELIA (LYME) TEST
K911599 IMMUNOWELL LYME (P39 RECOMBINANT) TEST
K911590 IMMUNOWELL BORRELIA (LYME)TEST
K914801 IMMUNOWELL DSDNA ANTIBODY TEST
K911848 IMMUNOWELL RNP/SM ANTIBODY TEST
K911851 IMMUNOWELL SM ANTIBODY TEST
K911849 IMMUNOWELL SJOGRENS SYNDROME A (RO)ANTIBODY TEST
Search all 23 clearances from General Biometrics, Inc. →