THEOPHYLLINE RIASSAY— 510(k) K792062

Substantially Equivalent

Ria Diagnostics

FDA 510(k) clearance K792062 for THEOPHYLLINE RIASSAY, Substantially Equivalent on 1980-02-25. Applicant: Ria Diagnostics. Device class: 2.

Clearance details

Applicant: Ria Diagnostics
Product code: Code LCA
Device class: Class 2
Regulation: 21 CFR 862.3880
Advisory panel: Clinical Toxicology
Date received: 1979-10-15
Decision date: 1980-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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