INFALERT— 510(k) K813507

Substantially Equivalent

Briox Technologies, Inc.

FDA 510(k) clearance K813507 for INFALERT, Substantially Equivalent on 1982-01-12. Applicant: Briox Technologies, Inc..

Clearance details

Applicant: Briox Technologies, Inc.
Product code: Code BZQ
Advisory panel: Anesthesiology
Date received: 1981-12-15
Decision date: 1982-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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