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

IMMUNOWELL SM ANTIBODY TEST

K Number: K911851 · Decision May 7, 1991
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
27
Applicant Total
23
Review Days
11

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Basic Information

Device Name
IMMUNOWELL SM ANTIBODY TEST
K Number
K911851
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
General Biometrics, Inc.
Date Received
April 26, 1991
Decision Date
May 7, 1991
Product Code
LKP
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
LKP Anti-Sm Antibody, Antigen And Control

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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
K911849 IMMUNOWELL SJOGRENS SYNDROME A (RO)ANTIBODY TEST
K911850 IMMUNWELL SJOGREN`S SYNDROME B (LA) ANTIBODY TEST
Search all 23 clearances from General Biometrics, Inc. →