Medical Device Manufacturer · IT , Casnate Con Bernate

Pikdare Spa - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

Pikdare Spa has 2 FDA 510(k) cleared medical devices. Based in Casnate Con Bernate, IT.

Last cleared in 2023. Active since 2022. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Pikdare Spa Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Pikdare Spa
2 devices
1-2 of 2
Cleared Jan 20, 2023
Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle
K203792 · FMI
General Hospital · 753d
Cleared Dec 02, 2022
DropSafeTM SicuraTM
K223353 · FMI
General Hospital · 30d
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