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FDA 510(k)

PINNACLE STAIR WAY LIFT

K-Number: K091858 · 2009-07-01

ApplicantSummit Harmar, LLC
Decision Date2009-07-01
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PINNACLE STAIR WAY LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Summit Harmar, LLC. It received FDA 510(k) clearance on 2009-07-01 under 510(k) number K091858. 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 PINNACLE STAIR WAY LIFT?

PINNACLE STAIR WAY LIFT is a medical device that received FDA 510(k) clearance on 2009-07-01. The listed applicant is Summit Harmar, LLC. The 510(k) number is K091858.

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

PINNACLE STAIR WAY LIFT received FDA 510(k) clearance on 2009-07-01, under 510(k) number K091858.

Who is the listed applicant for PINNACLE STAIR WAY LIFT?

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

What is the FDA product code for PINNACLE STAIR WAY LIFT?

The FDA product code for PINNACLE STAIR WAY LIFT is ILK.

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Related Devices (Code: ILK)

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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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