FDA 510(k)

8ch T/R Knee Coil

K-Number: K223225 · 2023-02-14

Decision Date2023-02-14

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

8ch T/R Knee Coil is a medical device manufactured by Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-02-14 under approval number K223225. 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 8ch T/R Knee Coil?

8ch T/R Knee Coil is a medical device that received FDA 510(k) clearance on 2023-02-14. It is manufactured by Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223225.

When was 8ch T/R Knee Coil approved by the FDA?

8ch T/R Knee Coil received FDA 510(k) clearance on 2023-02-14, under approval number K223225.

What company makes 8ch T/R Knee Coil?

8ch T/R Knee Coil is manufactured by Shenzhen RF Tech Co., Ltd..

What is the FDA product code for 8ch T/R Knee Coil?

The FDA product code for 8ch T/R Knee Coil is MOS.

Other Devices by Shenzhen RF Tech Co., Ltd.

K1609328ch Foot Ankle Coil K1609358ch Foot Ankle Coil K1722228ch Flex Suite K2008368ch Flex Suite K2232398ch Wrist Coil K2310851.5T HD T/R Knee Array (10-F34127)

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Related Devices (Code: MOS)

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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.