AIR PLUS AIR FLUIDIZED THERAPY SYSTEMS— 510(k) K852036

Name: FDA 510(k) clearance K852036
Creator: U.S. Food and Drug Administration
Published: 1985-09-05

Substantially Equivalent

Air Plus, Inc.

FDA 510(k) clearance K852036 for AIR PLUS AIR FLUIDIZED THERAPY SYSTEMS, Substantially Equivalent on 1985-09-05. Applicant: Air Plus, Inc.. Device class: 2.

Clearance details

Applicant: Air Plus, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1985-05-09
Decision date: 1985-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, 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.