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FDA 510(k)

joimax Endovapor 2

K-Number: K170358 · 2017-04-21

ApplicantJoimax GmbH
Decision Date2017-04-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

joimax Endovapor 2 is a medical device manufactured by Joimax GmbH. It received FDA 510(k) clearance on 2017-04-21 under approval number K170358. 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 Endovapor 2?

joimax Endovapor 2 is a medical device that received FDA 510(k) clearance on 2017-04-21. It is manufactured by Joimax GmbH. The 510(k) number is K170358.

When was joimax Endovapor 2 approved by the FDA?

joimax Endovapor 2 received FDA 510(k) clearance on 2017-04-21, under approval number K170358.

What company makes joimax Endovapor 2?

joimax Endovapor 2 is manufactured by Joimax GmbH.

What is the FDA product code for joimax Endovapor 2?

The FDA product code for joimax Endovapor 2 is GEI.

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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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