Oasis Lacrimal Intubation Set
K-Number: K160710 · 2016-05-13
Device Summary
Oasis Lacrimal Intubation Set is a medical device manufactured by Anodyne. It received FDA 510(k) clearance on 2016-05-13 under approval number K160710. The device is classified under product code OKS. FDA Decision: Unknown.
Frequently Asked Questions
What is the Oasis Lacrimal Intubation Set?
Oasis Lacrimal Intubation Set is a medical device that received FDA 510(k) clearance on 2016-05-13. It is manufactured by Anodyne. The 510(k) number is K160710.
When was Oasis Lacrimal Intubation Set approved by the FDA?
Oasis Lacrimal Intubation Set received FDA 510(k) clearance on 2016-05-13, under approval number K160710.
What company makes Oasis Lacrimal Intubation Set?
Oasis Lacrimal Intubation Set is manufactured by Anodyne.
What is the FDA product code for Oasis Lacrimal Intubation Set?
The FDA product code for Oasis Lacrimal Intubation Set is OKS.
Related Devices (Code: OKS)
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.