Medical Device Manufacturer · US , Las Vegas , NV

Marci Beauty, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Marci Beauty, Inc. has 1 FDA 510(k) cleared medical devices. Based in Las Vegas, US.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Marci Beauty, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Wenzhou Cytech Information Service Co., Ltd. as regulatory consultant.

FDA 510(k) Regulatory Record - Marci Beauty, Inc.
1 devices
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