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FDA 510(k)

SUMMIT STAIRWAY LIFT

K-Number: K032880 · 2003-11-10

ApplicantSummit Lifts, Inc.
Decision Date2003-11-10
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUMMIT STAIRWAY LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Summit Lifts, Inc.. It received FDA 510(k) clearance on 2003-11-10 under 510(k) number K032880. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUMMIT STAIRWAY LIFT?

SUMMIT STAIRWAY LIFT is a medical device that received FDA 510(k) clearance on 2003-11-10. The listed applicant is Summit Lifts, Inc.. The 510(k) number is K032880.

When did SUMMIT STAIRWAY LIFT receive FDA 510(k) clearance?

SUMMIT STAIRWAY LIFT received FDA 510(k) clearance on 2003-11-10, under 510(k) number K032880.

Who is the listed applicant for SUMMIT STAIRWAY LIFT?

The FDA 510(k) record lists Summit Lifts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUMMIT STAIRWAY LIFT?

The FDA product code for SUMMIT STAIRWAY LIFT is ILK.

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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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