INNOFLUOR PHENOBARBITAL ASSAY SYSTEM— 510(k) K972330

Substantially Equivalent

Oxis Intl., Inc.

FDA 510(k) clearance K972330 for INNOFLUOR PHENOBARBITAL ASSAY SYSTEM, Substantially Equivalent on 1997-07-14. Applicant: Oxis Intl., Inc..

Clearance details

Applicant: Oxis Intl., Inc.
Product code: Code LGQ
Advisory panel: Clinical Toxicology
Date received: 1997-06-23
Decision date: 1997-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

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