Philips IntelliSite Pathology Solution— 510(k) DEN160056
UnknownPhilips Medical Systems Nederland B.V.
FDA 510(k) clearance DEN160056 for Philips IntelliSite Pathology Solution, Unknown on 2017-04-12. Applicant: Philips Medical Systems Nederland B.V.. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems Nederland B.V.
- Product code
- Code PSY
- Device class
- Class 2
- Regulation
- 21 CFR 864.3700
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Best, NL
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Data sourced from openFDA. This site is unofficial and independent of the FDA.