AMERICAN PHARMASEAL HUMIDAIR CONDENSER— 510(k) K854012

Name: FDA 510(k) clearance K854012
Creator: U.S. Food and Drug Administration
Published: 1985-12-03

Substantially Equivalent

American Pharmaseal Div. Ahsc

FDA 510(k) clearance K854012 for AMERICAN PHARMASEAL HUMIDAIR CONDENSER, Substantially Equivalent on 1985-12-03. Applicant: American Pharmaseal Div. Ahsc. Device class: 1.

Clearance details

Applicant: American Pharmaseal Div. Ahsc
Product code: Code BYD
Device class: Class 1
Regulation: 21 CFR 868.5375
Advisory panel: Anesthesiology
Date received: 1985-09-30
Decision date: 1985-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

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