AV Vascular— 510(k) K253735
Substantially EquivalentPhilips Medical Systems Nederland B.V.
FDA 510(k) clearance K253735 for AV Vascular, Substantially Equivalent on 2026-01-22. Applicant: Philips Medical Systems Nederland B.V.. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems Nederland B.V.
- Product code
- Code QIH
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Best, NL
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Data sourced from openFDA. This site is unofficial and independent of the FDA.