FDA 510(k)

오아시스 눈물 duct 통신 세트

K-번호: K160710 · 2016-05-13

결정일2016-05-13

제품 코드OKS

결정Unknown

기기 요약

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.

자주 묻는 질문

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.

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오아시스 눈물 duct 통신 세트

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: OKS)

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