ClearLine IV— 510(k) K171954
Substantially EquivalentClearline MD
FDA 510(k) clearance K171954 for ClearLine IV, Substantially Equivalent on 2018-01-25. Applicant: Clearline MD. Device class: 2.
Clearance details
- Applicant
- Clearline MD
- Product code
- Code OKL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5445
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Woburn, MA, US
Recent devices under product code OKL
view allData sourced from openFDA. This site is unofficial and independent of the FDA.