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FDA 510(k)

STAIR-LIFT

K-Number: K981486 · 1998-07-01

ApplicantGaraventa (Canada) , Ltd.
Decision Date1998-07-01
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAIR-LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Garaventa (Canada) , Ltd.. It received FDA 510(k) clearance on 1998-07-01 under 510(k) number K981486. 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 STAIR-LIFT?

STAIR-LIFT is a medical device that received FDA 510(k) clearance on 1998-07-01. The listed applicant is Garaventa (Canada) , Ltd.. The 510(k) number is K981486.

When did STAIR-LIFT receive FDA 510(k) clearance?

STAIR-LIFT received FDA 510(k) clearance on 1998-07-01, under 510(k) number K981486.

Who is the listed applicant for STAIR-LIFT?

The FDA 510(k) record lists Garaventa (Canada) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAIR-LIFT?

The FDA product code for STAIR-LIFT 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, LLCK110495LIFTKAR PTSano Transportgerate GmbHK102088JOURNEY 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.

Official Source

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

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