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FDA 510(k)

Sunrise 6200, Sunrise 7200

K-Number: K173565 · 2018-02-14

ApplicantJk-Holding GmbH
Decision Date2018-02-14
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Sunrise 6200, Sunrise 7200 is a medical device manufactured by Jk-Holding GmbH. It received FDA 510(k) clearance on 2018-02-14 under approval number K173565. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sunrise 6200, Sunrise 7200?

Sunrise 6200, Sunrise 7200 is a medical device that received FDA 510(k) clearance on 2018-02-14. It is manufactured by Jk-Holding GmbH. The 510(k) number is K173565.

When was Sunrise 6200, Sunrise 7200 approved by the FDA?

Sunrise 6200, Sunrise 7200 received FDA 510(k) clearance on 2018-02-14, under approval number K173565.

What company makes Sunrise 6200, Sunrise 7200?

Sunrise 6200, Sunrise 7200 is manufactured by Jk-Holding GmbH.

What is the FDA product code for Sunrise 6200, Sunrise 7200?

The FDA product code for Sunrise 6200, Sunrise 7200 is LEJ.

Other Devices by Jk-Holding GmbH

K190173Ergoline Inspiration 550 Hybrid Technology / Sound, Ergoline Inspiration 550 Hybrid Technology / AC / Sound, Ergoline Planet Fitness 42/4 Hybrid Light Technology / Sound K183539Ergoline Sunrise 7200 Hybrid Technology K220500Ergoline Vitality Total Light 3, Planet Fitness 50/4 TLT by Ergoline, Planet Fitness 42/3 TLT by Ergoline, Ergoline Vitality Hybrid Light 3, Ergoline Vitality Hybrid Light, Planet Fitness 50/4 HLT by Ergoline, Planet Fitness 46/3 HLT by Ergoline, Ergoline Vitality Pure Light 3, Ergoline Vitality Pure Light, Planet Fitness 50/4 PLT III by Ergoline, Planet Fitness 50/4 PLT by Ergoline, Planet Fitness 46/3 PLT by Ergoline, Planet Fitness 42/3 PLT by Ergoline

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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.

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