pRESET LITE Thrombectomy Device— 510(k) K231539
Substantially EquivalentPhenox Limited
FDA 510(k) clearance K231539 for pRESET LITE Thrombectomy Device, Substantially Equivalent on 2023-10-21. Applicant: Phenox Limited.
Clearance details
- Applicant
- Phenox Limited
- Product code
- Code POL
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Galway, IE
Data sourced from openFDA. This site is unofficial and independent of the FDA.