STERI-AID KIT— 510(k) K963049

Substantially Equivalent

Steri-Aid, Inc.

FDA 510(k) clearance K963049 for STERI-AID KIT, Substantially Equivalent on 1996-11-12. Applicant: Steri-Aid, Inc.. Device class: 1.

Clearance details

Applicant: Steri-Aid, Inc.
Product code: Code FQZ
Device class: Class 1
Regulation: 21 CFR 880.2900
Advisory panel: General Hospital
Date received: 1996-07-25
Decision date: 1996-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North York,Ontario, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.