Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Ace Medical Devices Pvt. , Ltd.. It received FDA 510(k) clearance on 2016-07-11 under 510(k) 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. The listed applicant is Ace Medical Devices Pvt. , Ltd.. The 510(k) number is K153055.

When did ACE Electrosurgical Resection and Vaporization Electrodes Series receive FDA 510(k) clearance?

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

Who is the listed applicant for ACE Electrosurgical Resection and Vaporization Electrodes Series?

The FDA 510(k) record lists Ace Medical Devices Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

Related Devices (Code: GEI)

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.

K261179AlphaTriPart - Monopolar MIC InstrumentsGimmi GmbHK253504Volnewmer™Classys, Inc.K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S (TB-0520FCS)Olympus Medical Systems Corp.K253484LUTRONIC GENIUSCynosure Lutronic Technology CorporationK251492Irrigation Tubing Bipolar Cord SetNew Deantronics Taiwan , Ltd.K260636Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingStryker Sustainability Solutions

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.

↑