MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEM— 510(k) K881705

Name: FDA 510(k) clearance K881705
Creator: U.S. Food and Drug Administration
Published: 1988-07-13

Substantially Equivalent

Surgi-Med, Inc.

FDA 510(k) clearance K881705 for MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEM, Substantially Equivalent on 1988-07-13. Applicant: Surgi-Med, Inc.. Device class: 2.

Clearance details

Applicant: Surgi-Med, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1988-04-19
Decision date: 1988-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lansing, MI, US

Download summary PDF View on FDA.gov ↗

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