AMBU NEUROLINE DISPOSABLE INOJECT NEEDLE ELECTRODE— 510(k) K093825
Substantially EquivalentAmbu A/S
FDA 510(k) clearance K093825 for AMBU NEUROLINE DISPOSABLE INOJECT NEEDLE ELECTRODE, Substantially Equivalent on 2010-01-13. Applicant: Ambu A/S.
Clearance details
- Applicant
- Ambu A/S
- Product code
- Code IKT
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Glen Burnie, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.