TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE— 510(k) K905756

Name: FDA 510(k) clearance K905756
Creator: U.S. Food and Drug Administration
Published: 1991-01-08

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.. Device class: 2.

Clearance details

Applicant: Titan Technology Intl., Inc.
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
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

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.