joimax Electrosurgical Instruments
K-Number: K161378 · 2016-11-02
ApplicantJoimax GmbH
Decision Date2016-11-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
joimax Electrosurgical Instruments is a medical device manufactured by Joimax GmbH. It received FDA 510(k) clearance on 2016-11-02 under approval number K161378. 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 joimax Electrosurgical Instruments?
joimax Electrosurgical Instruments is a medical device that received FDA 510(k) clearance on 2016-11-02. It is manufactured by Joimax GmbH. The 510(k) number is K161378.
When was joimax Electrosurgical Instruments approved by the FDA?
joimax Electrosurgical Instruments received FDA 510(k) clearance on 2016-11-02, under approval number K161378.
What company makes joimax Electrosurgical Instruments?
joimax Electrosurgical Instruments is manufactured by Joimax GmbH.
What is the FDA product code for joimax Electrosurgical Instruments?
The FDA product code for joimax Electrosurgical Instruments is GEI.
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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.