Suzhou Microport Rehabtech (Group) Co., Ltd. - FDA 510(k) Cleared Dev...
1
Total
1
Cleared
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Denied
Suzhou Microport Rehabtech (Group) Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Suzhou, CN.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Suzhou Microport Rehabtech (Group) Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Microport Sinica Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Suzhou Microport Rehabtech (Group) Co., Ltd.
1 devices