CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002— 510(k) K922940

Name: FDA 510(k) clearance K922940
Creator: U.S. Food and Drug Administration
Published: 1992-10-05

Substantially Equivalent

Exos, Inc.

FDA 510(k) clearance K922940 for CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002, Substantially Equivalent on 1992-10-05. Applicant: Exos, Inc.. Device class: 2.

Clearance details

Applicant: Exos, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1992-06-18
Decision date: 1992-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woburn, MA, US

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