Decision Date2018-02-14
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Sunrise 6200, Sunrise 7200 is the device name listed in this FDA 510(k) record. The listed applicant is Jk-Holding GmbH. It received FDA 510(k) clearance on 2018-02-14 under 510(k) 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. The listed applicant is Jk-Holding GmbH. The 510(k) number is K173565.
When did Sunrise 6200, Sunrise 7200 receive FDA 510(k) clearance?
Sunrise 6200, Sunrise 7200 received FDA 510(k) clearance on 2018-02-14, under 510(k) number K173565.
Who is the listed applicant for Sunrise 6200, Sunrise 7200?
The FDA 510(k) record lists Jk-Holding GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sunrise 6200, Sunrise 7200?
The FDA product code for Sunrise 6200, Sunrise 7200 is LEJ.
Other records listing Jk-Holding GmbH as applicant
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Related Devices (Code: LEJ)
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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.