SENSIMED TRIGGERFISH— 510(k) DEN140017
UnknownSensimed AG
FDA 510(k) clearance DEN140017 for SENSIMED TRIGGERFISH, Unknown on 2016-03-04. Applicant: Sensimed AG. Device class: 2.
Clearance details
- Applicant
- Sensimed AG
- Product code
- Code PLZ
- Device class
- Class 2
- Regulation
- 21 CFR 886.1925
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Waltham, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.