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FDA 510(k)

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue

K-Number: K250482 · 2025-05-08

Decision Date2025-05-08
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue is a medical device manufactured by Fissiontech, LLC. It received FDA 510(k) clearance on 2025-05-08 under approval number K250482. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue?

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue is a medical device that received FDA 510(k) clearance on 2025-05-08. It is manufactured by Fissiontech, LLC. The 510(k) number is K250482.

When was Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue approved by the FDA?

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue received FDA 510(k) clearance on 2025-05-08, under approval number K250482.

What company makes Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue?

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue is manufactured by Fissiontech, LLC.

What is the FDA product code for Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue?

The FDA product code for Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue is LRK.

Related Clinical Trials

Related PubMed Literature

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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.