RXAIR 3000— 510(k) K951981

Substantially Equivalent

Clean Air Research & Development

FDA 510(k) clearance K951981 for RXAIR 3000, Substantially Equivalent on 1995-10-12. Applicant: Clean Air Research & Development. Device class: 2.

Clearance details

Applicant: Clean Air Research & Development
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 1995-04-27
Decision date: 1995-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, 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.