MEDI-PLINTH— 510(k) K924905

Name: FDA 510(k) clearance K924905
Creator: U.S. Food and Drug Administration
Published: 1993-02-16

Substantially Equivalent

Medi-Man Rehabilitation Products, Inc.

FDA 510(k) clearance K924905 for MEDI-PLINTH, Substantially Equivalent on 1993-02-16. Applicant: Medi-Man Rehabilitation Products, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Man Rehabilitation Products, Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1992-09-29
Decision date: 1993-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, L4w 1p4, CA

Download summary PDF View on FDA.gov ↗

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