Apinator
K-Number: K160123 · 2016-07-12
ApplicantAllen J. Moses, Dds, Ltd.
Decision Date2016-07-12
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Apinator is a medical device manufactured by Allen J. Moses, Dds, Ltd.. It received FDA 510(k) clearance on 2016-07-12 under approval number K160123. 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 Apinator?
Apinator is a medical device that received FDA 510(k) clearance on 2016-07-12. It is manufactured by Allen J. Moses, Dds, Ltd.. The 510(k) number is K160123.
When was Apinator approved by the FDA?
Apinator received FDA 510(k) clearance on 2016-07-12, under approval number K160123.
What company makes Apinator?
Apinator is manufactured by Allen J. Moses, Dds, Ltd..
What is the FDA product code for Apinator?
The FDA product code for Apinator 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.