The Panthera Anti-Snoring X3 Device
K-Number: K171576 · 2018-02-22
ApplicantPanthera Dental, Inc.
Decision Date2018-02-22
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
The Panthera Anti-Snoring X3 Device is a medical device manufactured by Panthera Dental, Inc.. It received FDA 510(k) clearance on 2018-02-22 under approval number K171576. 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 The Panthera Anti-Snoring X3 Device?
The Panthera Anti-Snoring X3 Device is a medical device that received FDA 510(k) clearance on 2018-02-22. It is manufactured by Panthera Dental, Inc.. The 510(k) number is K171576.
When was The Panthera Anti-Snoring X3 Device approved by the FDA?
The Panthera Anti-Snoring X3 Device received FDA 510(k) clearance on 2018-02-22, under approval number K171576.
What company makes The Panthera Anti-Snoring X3 Device?
The Panthera Anti-Snoring X3 Device is manufactured by Panthera Dental, Inc..
What is the FDA product code for The Panthera Anti-Snoring X3 Device?
The FDA product code for The Panthera Anti-Snoring X3 Device is LRK.
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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.