RONDEX CPR VALVE— 510(k) K855218

Substantially Equivalent

Kondex Products, Inc.

FDA 510(k) clearance K855218 for RONDEX CPR VALVE, Substantially Equivalent on 1986-02-12. Applicant: Kondex Products, Inc.. Device class: 2.

Clearance details

Applicant: Kondex Products, Inc.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1985-12-30
Decision date: 1986-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockford, IL, 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.