DigitalDiagnost C90
K-Number: K202564 · 2020-09-30
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2020-09-30
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
DigitalDiagnost C90 is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2020-09-30 under approval number K202564. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DigitalDiagnost C90?
DigitalDiagnost C90 is a medical device that received FDA 510(k) clearance on 2020-09-30. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K202564.
When was DigitalDiagnost C90 approved by the FDA?
DigitalDiagnost C90 received FDA 510(k) clearance on 2020-09-30, under approval number K202564.
What company makes DigitalDiagnost C90?
DigitalDiagnost C90 is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for DigitalDiagnost C90?
The FDA product code for DigitalDiagnost C90 is MQB.
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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.