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FDA 510(k)

LIFTKAR PT

K-Number: K110495 · 2011-05-20

ApplicantSano Transportgerate GmbH
Decision Date2011-05-20
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIFTKAR PT is the device name listed in this FDA 510(k) record. The listed applicant is Sano Transportgerate GmbH. It received FDA 510(k) clearance on 2011-05-20 under 510(k) number K110495. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFTKAR PT?

LIFTKAR PT is a medical device that received FDA 510(k) clearance on 2011-05-20. The listed applicant is Sano Transportgerate GmbH. The 510(k) number is K110495.

When did LIFTKAR PT receive FDA 510(k) clearance?

LIFTKAR PT received FDA 510(k) clearance on 2011-05-20, under 510(k) number K110495.

Who is the listed applicant for LIFTKAR PT?

The FDA 510(k) record lists Sano Transportgerate GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFTKAR PT?

The FDA product code for LIFTKAR PT is ING.

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Related Devices (Code: ING)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113065RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTSBella Elevator, LLCK102088JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFTThyssenkrupp Ceteco SrlK091881RPL/CPL VERTICAL PLATFORM LIFTSHarmar Summit, LLCK090856JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)Thyssenkrupp Ceteco SrlK073513MERITS E700 PORCE LIFTMerits Health Products Co., Ltd.K061514BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100Bruno Independent Living Aids, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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