dS FootAnkle Coil 8ch 1.5T
K-Number: K242096 · 2024-08-12
Decision Date2024-08-12
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
dS FootAnkle Coil 8ch 1.5T is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2024-08-12 under approval number K242096. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the dS FootAnkle Coil 8ch 1.5T?
dS FootAnkle Coil 8ch 1.5T is a medical device that received FDA 510(k) clearance on 2024-08-12. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K242096.
When was dS FootAnkle Coil 8ch 1.5T approved by the FDA?
dS FootAnkle Coil 8ch 1.5T received FDA 510(k) clearance on 2024-08-12, under approval number K242096.
What company makes dS FootAnkle Coil 8ch 1.5T?
dS FootAnkle Coil 8ch 1.5T is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for dS FootAnkle Coil 8ch 1.5T?
The FDA product code for dS FootAnkle Coil 8ch 1.5T is MOS.
Other Devices by Philips Medical Systems Nederland B.V.
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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.