Philips CombiDiagnost R90
K-Number: K163210 · 2017-01-31
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2017-01-31
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Philips CombiDiagnost R90 is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2017-01-31 under approval number K163210. 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 Philips CombiDiagnost R90?
Philips CombiDiagnost R90 is a medical device that received FDA 510(k) clearance on 2017-01-31. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K163210.
When was Philips CombiDiagnost R90 approved by the FDA?
Philips CombiDiagnost R90 received FDA 510(k) clearance on 2017-01-31, under approval number K163210.
What company makes Philips CombiDiagnost R90?
Philips CombiDiagnost R90 is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for Philips CombiDiagnost R90?
The FDA product code for Philips 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.