Oasis Lacrimal Intubation Set— 510(k) K160710

Unknown

Anodyne

FDA 510(k) clearance K160710 for Oasis Lacrimal Intubation Set, Unknown on 2016-05-13. Applicant: Anodyne.

Clearance details

Applicant: Anodyne
Product code: Code OKS
Advisory panel: Unknown
Date received: 2016-03-15
Decision date: 2016-05-13
Decision: Unknown
Clearance type: Traditional
Location: O' Fallon, MO, US

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