Zyppah Anti-Snoring Device
K-Number: K182312 · 2019-01-24
ApplicantAlways More Marketing
Decision Date2019-01-24
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Zyppah Anti-Snoring Device is a medical device manufactured by Always More Marketing. It received FDA 510(k) clearance on 2019-01-24 under approval number K182312. 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 Zyppah Anti-Snoring Device?
Zyppah Anti-Snoring Device is a medical device that received FDA 510(k) clearance on 2019-01-24. It is manufactured by Always More Marketing. The 510(k) number is K182312.
When was Zyppah Anti-Snoring Device approved by the FDA?
Zyppah Anti-Snoring Device received FDA 510(k) clearance on 2019-01-24, under approval number K182312.
What company makes Zyppah Anti-Snoring Device?
Zyppah Anti-Snoring Device is manufactured by Always More Marketing.
What is the FDA product code for Zyppah Anti-Snoring Device?
The FDA product code for Zyppah Anti-Snoring Device is LRK.
Related Clinical Trials
Related Devices (Code: LRK)
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.