K233204
- 510(k) number
- K233204
- Device name
- Philips IntelliSite Pathology Solution 5.1
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- PSY — Whole Slide Imaging System
- Decision date
- 2024-06-24
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 0.0 MB · U.S. public domain
Also available from FDA: K233204.pdf
Official FDA record: K233204
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.