ORTHOTIC LEG GAIT CORRECTOR DEVICE— 510(k) K800716

Name: FDA 510(k) clearance K800716
Creator: U.S. Food and Drug Administration
Published: 1980-05-02

Substantially Equivalent

Ipos Luneburg

FDA 510(k) clearance K800716 for ORTHOTIC LEG GAIT CORRECTOR DEVICE, Substantially Equivalent on 1980-05-02. Applicant: Ipos Luneburg. Device class: 1.

Clearance details

Applicant: Ipos Luneburg
Product code: Code ITO
Device class: Class 1
Regulation: 21 CFR 890.3410
Advisory panel: Physical Medicine
Date received: 1980-03-31
Decision date: 1980-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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