Radiography 7000 M
K-Number: K233678 · 2024-02-14
Device Summary
Frequently Asked Questions
What is the Radiography 7000 M?
Radiography 7000 M is a medical device that received FDA 510(k) clearance on 2024-02-14. The listed applicant is Philips Medical Systems Dmc GmbH. The 510(k) number is K233678.
When did Radiography 7000 M receive FDA 510(k) clearance?
Radiography 7000 M received FDA 510(k) clearance on 2024-02-14, under 510(k) number K233678.
Who is the listed applicant for Radiography 7000 M?
The FDA 510(k) record lists Philips Medical Systems Dmc GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Radiography 7000 M?
The FDA product code for Radiography 7000 M is IZL.
Other records listing Philips Medical Systems Dmc GmbH 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: IZL)
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.