510(k) K242096

dS FootAnkle Coil 8ch 1.5T by Philips Medical Systems Nederland B.V. — Product Code MOS

K242096 is an FDA 510(k) premarket notification submitted by Philips Medical Systems Nederland B.V. for the device "dS FootAnkle Coil 8ch 1.5T". The FDA issued a decision of Substantially Equivalent on August 12, 2024. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Philips Medical Systems Nederland B.V. has at least 10 other 510(k) clearances on record.