510(k) K230863

Device
ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM Control Kit
Applicant
Zeus Scientific
510(k) number
K230863
Product code
LSR
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-13
Date received
2023-03-29
Regulation
866.3830
Classification name
Reagent, Borrelia Serological Reagent
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
Mark Kopnitsky
Address
200 Evans Way Branchburg NJ US 08876 08876

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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