ProxiDiagnost N90
K-Number: K173433 · 2018-02-05
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2018-02-05
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ProxiDiagnost N90 is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2018-02-05 under approval number K173433. 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 ProxiDiagnost N90?
ProxiDiagnost N90 is a medical device that received FDA 510(k) clearance on 2018-02-05. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K173433.
When was ProxiDiagnost N90 approved by the FDA?
ProxiDiagnost N90 received FDA 510(k) clearance on 2018-02-05, under approval number K173433.
What company makes ProxiDiagnost N90?
ProxiDiagnost N90 is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for ProxiDiagnost N90?
The FDA product code for ProxiDiagnost N90 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.