FDA 510(k)

ZED Link

K-Number: K180549 · 2018-04-12

Decision Date2018-04-12

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ZED Link is the device name listed in this FDA 510(k) record. The listed applicant is Zed Technologies. It received FDA 510(k) clearance on 2018-04-12 under 510(k) number K180549. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZED Link?

ZED Link is a medical device that received FDA 510(k) clearance on 2018-04-12. The listed applicant is Zed Technologies. The 510(k) number is K180549.

When did ZED Link receive FDA 510(k) clearance?

ZED Link received FDA 510(k) clearance on 2018-04-12, under 510(k) number K180549.

Who is the listed applicant for ZED Link?

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

What is the FDA product code for ZED Link?

The FDA product code for ZED Link is LLZ.

Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.