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

IMMUNOWELL BORRELIA (LYME)TEST

K Number: K911590 · Decision Dec 20, 1991
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
110
Applicant Total
23
Review Days
255

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Basic Information

Device Name
IMMUNOWELL BORRELIA (LYME)TEST
K Number
K911590
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
General Biometrics, Inc.
Date Received
April 9, 1991
Decision Date
December 20, 1991
Product Code
LSR
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
LSR Reagent, Borrelia Serological Reagent

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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
K914801 IMMUNOWELL DSDNA ANTIBODY TEST
K911848 IMMUNOWELL RNP/SM ANTIBODY TEST
K911851 IMMUNOWELL 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. →