OBUS FORME ORTHOPEDIC BRACE, UPRIGHT— 510(k) K820051

Name: FDA 510(k) clearance K820051
Creator: U.S. Food and Drug Administration
Published: 1982-01-29

Substantially Equivalent

Obus Forme, Ltd.

FDA 510(k) clearance K820051 for OBUS FORME ORTHOPEDIC BRACE, UPRIGHT, Substantially Equivalent on 1982-01-29. Applicant: Obus Forme, Ltd.. Device class: 1.

Clearance details

Applicant: Obus Forme, Ltd.
Product code: Code IQE
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1982-01-08
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.