GARAVENTA X3 INCLINED PLATFORM LIFT— 510(k) K122206

Name: FDA 510(k) clearance K122206
Creator: U.S. Food and Drug Administration
Published: 2013-03-21

Substantially Equivalent

Garaventa (Canada) Ltd [Dba Garaventa Lift]

FDA 510(k) clearance K122206 for GARAVENTA X3 INCLINED PLATFORM LIFT, Substantially Equivalent on 2013-03-21. Applicant: Garaventa (Canada) Ltd [Dba Garaventa Lift]. Device class: 2.

Clearance details

Applicant: Garaventa (Canada) Ltd [Dba Garaventa Lift]
Product code: Code PCE
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 2012-07-25
Decision date: 2013-03-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Roswell, GA, US

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