REMUSK MP— 510(k) K922029

Substantially Equivalent

Equipement Biomedical Specialise, Inc.

FDA 510(k) clearance K922029 for REMUSK MP, Substantially Equivalent on 1992-10-06. Applicant: Equipement Biomedical Specialise, Inc..

Clearance details

Applicant: Equipement Biomedical Specialise, Inc.
Product code: Code LBB
Advisory panel: Orthopedic
Date received: 1992-05-01
Decision date: 1992-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

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