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FDA 510(k)

RPL/CPL VERTICAL PLATFORM LIFTS

K-Number: K091881 · 2009-07-01

Decision Date2009-07-01
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RPL/CPL VERTICAL PLATFORM LIFTS is the device name listed in this FDA 510(k) record. The listed applicant is Harmar Summit, LLC. It received FDA 510(k) clearance on 2009-07-01 under 510(k) number K091881. 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 RPL/CPL VERTICAL PLATFORM LIFTS?

RPL/CPL VERTICAL PLATFORM LIFTS is a medical device that received FDA 510(k) clearance on 2009-07-01. The listed applicant is Harmar Summit, LLC. The 510(k) number is K091881.

When did RPL/CPL VERTICAL PLATFORM LIFTS receive FDA 510(k) clearance?

RPL/CPL VERTICAL PLATFORM LIFTS received FDA 510(k) clearance on 2009-07-01, under 510(k) number K091881.

Who is the listed applicant for RPL/CPL VERTICAL PLATFORM LIFTS?

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

What is the FDA product code for RPL/CPL VERTICAL PLATFORM LIFTS?

The FDA product code for RPL/CPL VERTICAL PLATFORM LIFTS is ING.

Related Clinical Trials

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.

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.

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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