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

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG Test System

K Number: K191398 · Decision Jul 29, 2019
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
110
Applicant Total
135
Review Days
66

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Basic Information

Device Name
ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG Test System
K Number
K191398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zeus Scientific, Inc.
Date Received
May 24, 2019
Decision Date
July 29, 2019
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 Zeus Scientific, Inc.

K Number Device Name
K201956 Zeus IFA ANA HEp-2 Test System, Zeus dIFine
K190907 ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG/IgM Test System
K191240 ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System
K113397 ZEUS ELISA BORRELIA VLSE-1/PEPC10 IGG/IGM TEST SYSTEM
K102425 ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM
K103603 ZEUS ELISA HSV GG-2 IGG TEST SYSTEM
K103363 ZEUS ELISA HSV GC-I IGG TEST SYSTEM
K102283 ZEUS SCIENTIFIC, INC. TREPONEMA PALLIDUM IGG TEST SYSTEM
K093784 ATHENA MULTI-LYTE TORCH IGG PLUS TEST SYSTEM
K100728 ATHENA MULTI-LYTE BORRELIA VLSE-1/PEPC10 PLUS TEST SYSTEM
Search all 135 clearances from Zeus Scientific, Inc. →