510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122206Substantially Equivalent

Garaventa X3 Inclined Platform Lift

Garaventa (Canada) Ltd [dba Garaventa Lift], Roswell GA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122206 is the FDA 510(k) clearance record for GARAVENTA X3 INCLINED PLATFORM LIFT, a class II device, cleared for Garaventa (Canada) Ltd [Dba Garaventa Lift] on under FDA product code PCE (Permanently Mounted Wheelchair Platform Lift). FDA's definition for product code PCE reads: "Intended for medical purposes to provide a guided platform to move a person with impaired mobility, with or without a wheelchair, from one level to another". FDA records list one 510(k) clearance for Garaventa (Canada) Ltd [Dba Garaventa Lift]. As of , FDA records show no recalls naming K122206.

Clearance record

Decision date
Received
(239 days to decision)
Product code
PCE Permanently Mounted Wheelchair Platform Lift
Regulation
21 CFR 890.3930
Device class
Class II
Review panel
Physical Medicine
Applicant
Garaventa (Canada) Ltd [Dba Garaventa Lift] 845 Aronson Lake Ct., Roswell GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PCE

Trailing 12 months

FDA records hold no clearances under product code PCE in the trailing twelve months.

FDA records show no clearances under product code PCE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code PCE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260