Zenition 30
K-Number: K232420 · 2024-02-16
Decision Date2024-02-16
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Zenition 30 is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2024-02-16 under approval number K232420. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Zenition 30?
Zenition 30 is a medical device that received FDA 510(k) clearance on 2024-02-16. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K232420.
When was Zenition 30 approved by the FDA?
Zenition 30 received FDA 510(k) clearance on 2024-02-16, under approval number K232420.
What company makes Zenition 30?
Zenition 30 is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for Zenition 30?
The FDA product code for Zenition 30 is OWB.
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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.