RESUSCITATOR VALVE ASSEMBLY W/FILTER— 510(k) K882204

Name: FDA 510(k) clearance K882204
Creator: U.S. Food and Drug Administration
Published: 1988-07-08

Substantially Equivalent

Intertech/Ohio

FDA 510(k) clearance K882204 for RESUSCITATOR VALVE ASSEMBLY W/FILTER, Substantially Equivalent on 1988-07-08. Applicant: Intertech/Ohio. Device class: 2.

Clearance details

Applicant: Intertech/Ohio
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1988-05-25
Decision date: 1988-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Myers, FL, US

Download summary PDF View on FDA.gov ↗

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