FDA 510(k)

Oasis Lacrimal Intubation Set

K-Number: K160710 · 2016-05-13

Decision Date2016-05-13

Product CodeOKS

DecisionUnknown

Device Summary

Oasis Lacrimal Intubation Set is the device name listed in this FDA 510(k) record. The listed applicant is Anodyne. It received FDA 510(k) clearance on 2016-05-13 under 510(k) 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. The listed applicant is Anodyne. The 510(k) number is K160710.

When did Oasis Lacrimal Intubation Set receive FDA 510(k) clearance?

Oasis Lacrimal Intubation Set received FDA 510(k) clearance on 2016-05-13, under 510(k) number K160710.

Who is the listed applicant for Oasis Lacrimal Intubation Set?

The FDA 510(k) record lists Anodyne as the applicant. This does not by itself establish the device manufacturer.

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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) Sas K201606LacriJet®Fci (France Chirurgie Instrumentation) Sas K170247Lacriflow CLKaneka Pharma America, LLC K161373NunchakuFci (France Chirurgie Instrumentation)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.