Radiography 7300 C
K-Number: K233662 · 2024-06-13
ApplicantPhilips Medical Systems Dmc GmbH
Decision Date2024-06-13
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Radiography 7300 C is a medical device manufactured by Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2024-06-13 under approval number K233662. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Radiography 7300 C?
Radiography 7300 C is a medical device that received FDA 510(k) clearance on 2024-06-13. It is manufactured by Philips Medical Systems Dmc GmbH. The 510(k) number is K233662.
When was Radiography 7300 C approved by the FDA?
Radiography 7300 C received FDA 510(k) clearance on 2024-06-13, under approval number K233662.
What company makes Radiography 7300 C?
Radiography 7300 C is manufactured by Philips Medical Systems Dmc GmbH.
What is the FDA product code for Radiography 7300 C?
The FDA product code for Radiography 7300 C is KPR.
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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.