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FDA 510(k)

ACE Electrosurgical Resection and Vaporization Electrodes Series

K-Number: K153055 · 2016-07-11

ApplicantAce Medical Devices Pvt. , Ltd.
Decision Date2016-07-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACE Electrosurgical Resection and Vaporization Electrodes Series is a medical device manufactured by Ace Medical Devices Pvt. , Ltd.. It received FDA 510(k) clearance on 2016-07-11 under approval number K153055. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE Electrosurgical Resection and Vaporization Electrodes Series?

ACE Electrosurgical Resection and Vaporization Electrodes Series is a medical device that received FDA 510(k) clearance on 2016-07-11. It is manufactured by Ace Medical Devices Pvt. , Ltd.. The 510(k) number is K153055.

When was ACE Electrosurgical Resection and Vaporization Electrodes Series approved by the FDA?

ACE Electrosurgical Resection and Vaporization Electrodes Series received FDA 510(k) clearance on 2016-07-11, under approval number K153055.

What company makes ACE Electrosurgical Resection and Vaporization Electrodes Series?

ACE Electrosurgical Resection and Vaporization Electrodes Series is manufactured by Ace Medical Devices Pvt. , Ltd..

What is the FDA product code for ACE Electrosurgical Resection and Vaporization Electrodes Series?

The FDA product code for ACE Electrosurgical Resection and Vaporization Electrodes Series is GEI.

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Official Source

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