CLINICAL HANDMASTER SYSTEM OR CHMS— 510(k) K914436

Name: FDA 510(k) clearance K914436
Creator: U.S. Food and Drug Administration
Published: 1992-01-02

Substantially Equivalent

Exos Medical Products

FDA 510(k) clearance K914436 for CLINICAL HANDMASTER SYSTEM OR CHMS, Substantially Equivalent on 1992-01-02. Applicant: Exos Medical Products. Device class: 2.

Clearance details

Applicant: Exos Medical Products
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1991-10-04
Decision date: 1992-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

Download summary PDF View on FDA.gov ↗

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