Radiography 7000 M
K-Number: K233678 · 2024-02-14
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2024-02-14
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Radiography 7000 M is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2024-02-14 under approval number K233678. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K233678.
When was Radiography 7000 M approved by the FDA?
Radiography 7000 M received FDA 510(k) clearance on 2024-02-14, under approval number K233678.
What company makes Radiography 7000 M?
Radiography 7000 M is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for Radiography 7000 M?
The FDA product code for Radiography 7000 M is IZL.
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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.