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

ZEUS ELISA HSV GC-I IGG TEST SYSTEM

K Number: K103363 · Decision Apr 26, 2011
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
19
Applicant Total
135
Review Days
160

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Basic Information

Device Name
ZEUS ELISA HSV GC-I IGG TEST SYSTEM
K Number
K103363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zeus Scientific, Inc.
Date Received
November 17, 2010
Decision Date
April 26, 2011
Product Code
MXJ
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
MXJ Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1

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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
K191398 ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG 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
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. →