STAGE IV, AIR-FLUIDIZE BED— 510(k) K904008

Name: FDA 510(k) clearance K904008
Creator: U.S. Food and Drug Administration
Published: 1990-10-10

Substantially Equivalent

Unique Flotation Systems, Inc.

FDA 510(k) clearance K904008 for STAGE IV, AIR-FLUIDIZE BED, Substantially Equivalent on 1990-10-10. Applicant: Unique Flotation Systems, Inc.. Device class: 2.

Clearance details

Applicant: Unique Flotation Systems, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1990-08-29
Decision date: 1990-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Corona, CA, US

Download summary PDF View on FDA.gov ↗

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