DeviceClearance

HERPES VIRUS HOMINIS ANTIBODY TEST SYS.— 510(k) K812085

Substantially Equivalent

Zeus Scientific, Inc.

FDA 510(k) clearance K812085 for HERPES VIRUS HOMINIS ANTIBODY TEST SYS., Substantially Equivalent on 1981-09-01. Applicant: Zeus Scientific, Inc..

Clearance details

Applicant
Zeus Scientific, Inc.
Product code
Code GQL
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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