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 a medical device manufactured by Ge Hangwei Medical Systems Co., Ltd.. It received FDA 510(k) clearance on 2024-02-22 under approval 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. It is manufactured by Ge Hangwei Medical Systems Co., Ltd.. The 510(k) number is K233749.
When was Revolution Ascend Sliding approved by the FDA?
Revolution Ascend Sliding received FDA 510(k) clearance on 2024-02-22, under approval number K233749.
What company makes Revolution Ascend Sliding?
Revolution Ascend Sliding is manufactured by Ge Hangwei Medical Systems Co., Ltd..
What is the FDA product code for Revolution Ascend Sliding?
The FDA product code for Revolution Ascend Sliding is JAK.
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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.