CombiDiagnost R90
K-Number: K203087 · 2020-12-03
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2020-12-03
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CombiDiagnost R90 is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2020-12-03 under approval number K203087. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CombiDiagnost R90?
CombiDiagnost R90 is a medical device that received FDA 510(k) clearance on 2020-12-03. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K203087.
When was CombiDiagnost R90 approved by the FDA?
CombiDiagnost R90 received FDA 510(k) clearance on 2020-12-03, under approval number K203087.
What company makes CombiDiagnost R90?
CombiDiagnost R90 is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for CombiDiagnost R90?
The FDA product code for CombiDiagnost R90 is JAA.
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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.