ORLAU SWIVEL WALKER— 510(k) K923880

Substantially Equivalent

Mopac, Ltd.

FDA 510(k) clearance K923880 for ORLAU SWIVEL WALKER, Substantially Equivalent on 1996-09-30. Applicant: Mopac, Ltd.. Device class: 1.

Clearance details

Applicant: Mopac, Ltd.
Product code: Code MRI
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1992-07-31
Decision date: 1996-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eau Claire, WI, US

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