Spectral CT 7500 RT
K-Number: K240844 · 2024-10-18
Decision Date2024-10-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Spectral CT 7500 RT is a medical device manufactured by Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2024-10-18 under approval number K240844. 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 Spectral CT 7500 RT?
Spectral CT 7500 RT is a medical device that received FDA 510(k) clearance on 2024-10-18. It is manufactured by Philips Medical Systems Technologies , Ltd.. The 510(k) number is K240844.
When was Spectral CT 7500 RT approved by the FDA?
Spectral CT 7500 RT received FDA 510(k) clearance on 2024-10-18, under approval number K240844.
What company makes Spectral CT 7500 RT?
Spectral CT 7500 RT is manufactured by Philips Medical Systems Technologies , Ltd..
What is the FDA product code for Spectral CT 7500 RT?
The FDA product code for Spectral CT 7500 RT 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.