Snore Bandit
K-Number: K210910 · 2021-07-01
ApplicantSnorebandit, LLC
Decision Date2021-07-01
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Snore Bandit is a medical device manufactured by Snorebandit, LLC. It received FDA 510(k) clearance on 2021-07-01 under approval number K210910. 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 Snore Bandit?
Snore Bandit is a medical device that received FDA 510(k) clearance on 2021-07-01. It is manufactured by Snorebandit, LLC. The 510(k) number is K210910.
When was Snore Bandit approved by the FDA?
Snore Bandit received FDA 510(k) clearance on 2021-07-01, under approval number K210910.
What company makes Snore Bandit?
Snore Bandit is manufactured by Snorebandit, LLC.
What is the FDA product code for Snore Bandit?
The FDA product code for Snore Bandit is LRK.
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.