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FDA 510(k)

JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT

K-Number: K102088 · 2010-10-20

Decision Date2010-10-20
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Thyssenkrupp Ceteco Srl. It received FDA 510(k) clearance on 2010-10-20 under 510(k) number K102088. 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 JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT?

JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT is a medical device that received FDA 510(k) clearance on 2010-10-20. The listed applicant is Thyssenkrupp Ceteco Srl. The 510(k) number is K102088.

When did JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT receive FDA 510(k) clearance?

JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT received FDA 510(k) clearance on 2010-10-20, under 510(k) number K102088.

Who is the listed applicant for JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT?

The FDA 510(k) record lists Thyssenkrupp Ceteco Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT?

The FDA product code for JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT 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.

Other records listing Thyssenkrupp Ceteco Srl as applicant

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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