Oasis Lacrimal Intubation Set— 510(k) K160710
UnknownAnodyne
FDA 510(k) clearance K160710 for Oasis Lacrimal Intubation Set, Unknown on 2016-05-13. Applicant: Anodyne. Device class: Unclassified.
Clearance details
- Applicant
- Anodyne
- Product code
- Code OKS
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- O' Fallon, MO, US
Recent devices under product code OKS
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