Philips IntelliSite Pathology Solution 5.1— 510(k) K233204
Substantially EquivalentPhilips Medical Systems Nederland B.V.
FDA 510(k) clearance K233204 for Philips IntelliSite Pathology Solution 5.1, Substantially Equivalent on 2024-06-24. Applicant: Philips Medical Systems Nederland B.V..
Clearance details
- Applicant
- Philips Medical Systems Nederland B.V.
- Product code
- Code PSY
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Best, NL
Data sourced from openFDA. This site is unofficial and independent of the FDA.