LIFTKAR PT— 510(k) K110495

Name: FDA 510(k) clearance K110495
Creator: U.S. Food and Drug Administration
Published: 2011-05-20

Substantially Equivalent

Sano Transportgerate GmbH

FDA 510(k) clearance K110495 for LIFTKAR PT, Substantially Equivalent on 2011-05-20. Applicant: Sano Transportgerate GmbH. Device class: 2.

Clearance details

Applicant: Sano Transportgerate GmbH
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 2011-02-22
Decision date: 2011-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Downers Grove, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ING

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K113065 — RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTS2012-02-22
K102088 — JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT2010-10-20
K091881 — RPL/CPL VERTICAL PLATFORM LIFTS2009-07-01
K090856 — JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)2009-05-27
K073513 — MERITS E700 PORCE LIFT2008-01-14

Adverse events under product code ING

product code ING

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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