FDA 510(k)

8ch Flex Suite

K-Number: K200836 · 2020-07-22

Decision Date2020-07-22

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

8ch Flex Suite is a medical device manufactured by Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2020-07-22 under approval number K200836. 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 Flex Suite?

8ch Flex Suite is a medical device that received FDA 510(k) clearance on 2020-07-22. It is manufactured by Shenzhen RF Tech Co., Ltd.. The 510(k) number is K200836.

When was 8ch Flex Suite approved by the FDA?

8ch Flex Suite received FDA 510(k) clearance on 2020-07-22, under approval number K200836.

What company makes 8ch Flex Suite?

8ch Flex Suite is manufactured by Shenzhen RF Tech Co., Ltd..

What is the FDA product code for 8ch Flex Suite?

The FDA product code for 8ch Flex Suite is MOS.

Other Devices by Shenzhen RF Tech Co., Ltd.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.