FDA 510(k)

8ch Bobina de Pie y Tobillo

N.º K: K160935 · 2016-07-28

Fecha de decisión2016-07-28

Código de productoMOS

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

8ch Foot Ankle Coil is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2016-07-28 under 510(k) number K160935. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the 8ch Foot Ankle Coil?

8ch Foot Ankle Coil is a medical device that received FDA 510(k) clearance on 2016-07-28. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K160935.

When did 8ch Foot Ankle Coil receive FDA 510(k) clearance?

8ch Foot Ankle Coil received FDA 510(k) clearance on 2016-07-28, under 510(k) number K160935.

Who is the listed applicant for 8ch Foot Ankle Coil?

The FDA 510(k) record lists Shenzhen RF Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 8ch Foot Ankle Coil?

The FDA product code for 8ch Foot Ankle Coil is MOS.

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Otros registros que enlistan a Shenzhen RF Tech Co., Ltd. como solicitante

K252587HD 8Ch Wrist Array K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive Only K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive Only K2310851.5T HD T/R Knee Array (10-F34127)K2232031.5T 24E Posterior Array K2232258ch Bobina de Rodilla T/R

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Dispositivos relacionados (Código: MOS)

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Fuente oficial

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