Spectral CT 7500 RT
K-Number: K240844 · 2024-10-18
Device Summary
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. The listed applicant is Philips Medical Systems Technologies , Ltd.. The 510(k) number is K240844.
When did Spectral CT 7500 RT receive FDA 510(k) clearance?
Spectral CT 7500 RT received FDA 510(k) clearance on 2024-10-18, under 510(k) number K240844.
Who is the listed applicant for Spectral CT 7500 RT?
The FDA 510(k) record lists Philips Medical Systems Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spectral CT 7500 RT?
The FDA product code for Spectral CT 7500 RT is JAK.
Other records listing Philips Medical Systems Technologies , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JAK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.