Vital Sleep
K-Number: K201719 · 2021-01-14
ApplicantThe Snore Reliever Company, LLC
Decision Date2021-01-14
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Vital Sleep is a medical device manufactured by The Snore Reliever Company, LLC. It received FDA 510(k) clearance on 2021-01-14 under approval number K201719. 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 Vital Sleep?
Vital Sleep is a medical device that received FDA 510(k) clearance on 2021-01-14. It is manufactured by The Snore Reliever Company, LLC. The 510(k) number is K201719.
When was Vital Sleep approved by the FDA?
Vital Sleep received FDA 510(k) clearance on 2021-01-14, under approval number K201719.
What company makes Vital Sleep?
Vital Sleep is manufactured by The Snore Reliever Company, LLC.
What is the FDA product code for Vital Sleep?
The FDA product code for Vital Sleep 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.