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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 a medical device manufactured by Nexsys Electronics Inc. Dba Medweb. It received FDA 510(k) clearance on 2024-12-20 under approval 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. It is manufactured by Nexsys Electronics Inc. Dba Medweb. The 510(k) number is K242362.

When was Lightning Viewer approved by the FDA?

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

What company makes Lightning Viewer?

Lightning Viewer is manufactured by Nexsys Electronics Inc. Dba Medweb.

What is the FDA product code for Lightning Viewer?

The FDA product code for Lightning Viewer is LLZ.

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Official Source

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