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.

FDA 510(k) cleared devices by 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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