FDA 510(k)

Lightning Viewer

K-Number: K242362 · 2024-12-20

ApplicantNexsys Electronics Inc. Dba Medweb

Decision Date2024-12-20

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Lightning Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Nexsys Electronics Inc. Dba Medweb. It received FDA 510(k) clearance on 2024-12-20 under 510(k) number K242362. 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 Lightning Viewer?

Lightning Viewer is a medical device that received FDA 510(k) clearance on 2024-12-20. The listed applicant is Nexsys Electronics Inc. Dba Medweb. The 510(k) number is K242362.

When did Lightning Viewer receive FDA 510(k) clearance?

Lightning Viewer received FDA 510(k) clearance on 2024-12-20, under 510(k) number K242362.

Who is the listed applicant for Lightning Viewer?

The FDA 510(k) record lists Nexsys Electronics Inc. Dba Medweb as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lightning Viewer?

The FDA product code for Lightning Viewer 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.