DIRECT FA CONJUGATE FOR LEGIONELLA SPP— 510(k) K822859

Name: FDA 510(k) clearance K822859
Creator: U.S. Food and Drug Administration
Published: 1983-02-16

Substantially Equivalent

Zeus Technologies

FDA 510(k) clearance K822859 for DIRECT FA CONJUGATE FOR LEGIONELLA SPP, Substantially Equivalent on 1983-02-16. Applicant: Zeus Technologies. Device class: 2.

Clearance details

Applicant: Zeus Technologies
Product code: Code LHL
Device class: Class 2
Regulation: 21 CFR 866.3300
Advisory panel: Microbiology
Date received: 1982-09-27
Decision date: 1983-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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