Sonopuls 190— 510(k) K230472
Substantially EquivalentEnraf-Nonius, B.V.
FDA 510(k) clearance K230472 for Sonopuls 190, Substantially Equivalent on 2023-10-24. Applicant: Enraf-Nonius, B.V.. Device class: 2.
Clearance details
- Applicant
- Enraf-Nonius, B.V.
- Product code
- Code IMI
- Device class
- Class 2
- Regulation
- 21 CFR 890.5300
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rotterdam, NL
Recent devices under product code IMI
view allMore clearances from Enraf-Nonius, B.V.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.