Philips Ingenuity CT
K-Number: K160743 · 2016-08-08
Decision Date2016-08-08
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Philips Ingenuity CT is a medical device manufactured by Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 2016-08-08 under approval number K160743. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Philips Ingenuity CT?
Philips Ingenuity CT is a medical device that received FDA 510(k) clearance on 2016-08-08. It is manufactured by Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K160743.
When was Philips Ingenuity CT approved by the FDA?
Philips Ingenuity CT received FDA 510(k) clearance on 2016-08-08, under approval number K160743.
What company makes Philips Ingenuity CT?
Philips Ingenuity CT is manufactured by Philips Medical Systems (Cleveland), Inc..
What is the FDA product code for Philips Ingenuity CT?
The FDA product code for Philips Ingenuity CT is JAK.
Other Devices by Philips Medical Systems (Cleveland), Inc.
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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.