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FDA 510(k)

Revolution Ascend Sliding

K-Number: K233749 · 2024-02-22

ApplicantGe Hangwei Medical Systems Co., Ltd.
Decision Date2024-02-22
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Revolution Ascend Sliding is the device name listed in this FDA 510(k) record. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K233749. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Revolution Ascend Sliding?

Revolution Ascend Sliding is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. The 510(k) number is K233749.

When did Revolution Ascend Sliding receive FDA 510(k) clearance?

Revolution Ascend Sliding received FDA 510(k) clearance on 2024-02-22, under 510(k) number K233749.

Who is the listed applicant for Revolution Ascend Sliding?

The FDA 510(k) record lists Ge Hangwei Medical Systems Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Revolution Ascend Sliding?

The FDA product code for Revolution Ascend Sliding is JAK.

Other records listing Ge Hangwei Medical Systems Co., Ltd. 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.

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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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