CLINITRON AIR FLUIDIZED SUPPORT SYSTEM— 510(k) K813584

Name: FDA 510(k) clearance K813584
Creator: U.S. Food and Drug Administration
Published: 1982-01-12

Substantially Equivalent

Uhi Corp.

FDA 510(k) clearance K813584 for CLINITRON AIR FLUIDIZED SUPPORT SYSTEM, Substantially Equivalent on 1982-01-12. Applicant: Uhi Corp.. Device class: 2.

Clearance details

Applicant: Uhi Corp.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1981-12-28
Decision date: 1982-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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