MICROAIR FLUIDIZED AIR BED— 510(k) K884529

Substantially Equivalent

Gsi Development Co.

FDA 510(k) clearance K884529 for MICROAIR FLUIDIZED AIR BED, Substantially Equivalent on 1988-11-18. Applicant: Gsi Development Co.. Device class: 2.

Clearance details

Applicant: Gsi Development Co.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1988-10-28
Decision date: 1988-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carmel, NY, US

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