TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE— 510(k) K905756

Substantially Equivalent

Titan Technology Intl., Inc.

FDA 510(k) clearance K905756 for TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE, Substantially Equivalent on 1991-01-08. Applicant: Titan Technology Intl., Inc..

Clearance details

Applicant: Titan Technology Intl., Inc.
Product code: Code JFB
Advisory panel: Physical Medicine
Date received: 1990-12-27
Decision date: 1991-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MI, US

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