SnoreRx
K-Number: K153200 · 2016-08-09
ApplicantApnea Sciences Corporation
Decision Date2016-08-09
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
SnoreRx is a medical device manufactured by Apnea Sciences Corporation. It received FDA 510(k) clearance on 2016-08-09 under approval number K153200. 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 SnoreRx?
SnoreRx is a medical device that received FDA 510(k) clearance on 2016-08-09. It is manufactured by Apnea Sciences Corporation. The 510(k) number is K153200.
When was SnoreRx approved by the FDA?
SnoreRx received FDA 510(k) clearance on 2016-08-09, under approval number K153200.
What company makes SnoreRx?
SnoreRx is manufactured by Apnea Sciences Corporation.
What is the FDA product code for SnoreRx?
The FDA product code for SnoreRx is LRK.
Other Devices by Apnea Sciences Corporation
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.