Philips Incisive CT on Trailer
K-Number: K211168 · 2021-11-22
Decision Date2021-11-22
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Philips Incisive CT on Trailer is a medical device manufactured by Philips Healthcare (Suzhou) Co., Ltd.. It received FDA 510(k) clearance on 2021-11-22 under approval number K211168. 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 Incisive CT on Trailer?
Philips Incisive CT on Trailer is a medical device that received FDA 510(k) clearance on 2021-11-22. It is manufactured by Philips Healthcare (Suzhou) Co., Ltd.. The 510(k) number is K211168.
When was Philips Incisive CT on Trailer approved by the FDA?
Philips Incisive CT on Trailer received FDA 510(k) clearance on 2021-11-22, under approval number K211168.
What company makes Philips Incisive CT on Trailer?
Philips Incisive CT on Trailer is manufactured by Philips Healthcare (Suzhou) Co., Ltd..
What is the FDA product code for Philips Incisive CT on Trailer?
The FDA product code for Philips Incisive CT on Trailer is JAK.
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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.