Medical Device Manufacturer · US , Sunny Isles Beach , FL

Silq Technologies, Corp. - FDA 510(k) Cleared Devices

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

Silq Technologies, Corp. has 1 FDA 510(k) cleared medical devices. Based in Sunny Isles Beach, US.

Last cleared in 2022. Active since 2022. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Silq Technologies, Corp. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Pathway, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Silq Technologies, Corp.
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