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

IMMUMODOT AUTOIMMUNITY SCREENING PANEL 4

K Number: K903047 · Decision Aug 9, 1990
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
23
Review Days
29

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Basic Information

Device Name
IMMUMODOT AUTOIMMUNITY SCREENING PANEL 4
K Number
K903047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
General Biometrics, Inc.
Date Received
July 11, 1990
Decision Date
August 9, 1990
Product Code
LLL
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
LLL Extractable Antinuclear Antibody, Antigen And Control

Similar 510(k) Clearances

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

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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. →