INNOFLUOR THEOPHYLLINE ASSAY SYSTEM— 510(k) K955567

Substantially Equivalent

Oxis Intl., Inc.

FDA 510(k) clearance K955567 for INNOFLUOR THEOPHYLLINE ASSAY SYSTEM, Substantially Equivalent on 1996-01-24. Applicant: Oxis Intl., Inc..

Clearance details

Applicant: Oxis Intl., Inc.
Product code: Code LGS
Advisory panel: Clinical Toxicology
Date received: 1995-12-06
Decision date: 1996-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

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