Philips IntelliSite Pathology Solution 5.1
K-Number: K233204 · 2024-06-24
Decision Date2024-06-24
Product CodePSY
Advisory CommitteePA
DecisionSubstantially Equivalent
Device Summary
Philips IntelliSite Pathology Solution 5.1 is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2024-06-24 under approval number K233204. The device is classified under product code PSY. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Philips IntelliSite Pathology Solution 5.1?
Philips IntelliSite Pathology Solution 5.1 is a medical device that received FDA 510(k) clearance on 2024-06-24. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K233204.
When was Philips IntelliSite Pathology Solution 5.1 approved by the FDA?
Philips IntelliSite Pathology Solution 5.1 received FDA 510(k) clearance on 2024-06-24, under approval number K233204.
What company makes Philips IntelliSite Pathology Solution 5.1?
Philips IntelliSite Pathology Solution 5.1 is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for Philips IntelliSite Pathology Solution 5.1?
The FDA product code for Philips IntelliSite Pathology Solution 5.1 is PSY.
Related Clinical Trials
Other Devices by Philips Medical Systems Nederland B.V.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.