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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 the device name listed in this FDA 510(k) record. The listed applicant is Joimax GmbH. It received FDA 510(k) clearance on 2017-04-21 under 510(k) 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. The listed applicant is Joimax GmbH. The 510(k) number is K170358.

When did joimax Endovapor 2 receive FDA 510(k) clearance?

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

Who is the listed applicant for joimax Endovapor 2?

The FDA 510(k) record lists Joimax GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for joimax Endovapor 2?

The FDA product code for joimax Endovapor 2 is GEI.

Other records listing Joimax GmbH as applicant

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.

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Related Devices (Code: 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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