Medical Device Manufacturer · US , Morton , PA

Pressure Products Medical Device Manufacturing, LLC - FDA 510(k) Clea...

9 submissions · 9 cleared · Since 2017

Recent clearances: SafeSept RF Transseptal Guidewire (SSRF132, SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198), SafeSept® Transseptal Guidewire (SS-140)

9
Total
9
Cleared
0
Denied

Pressure Products Medical Device Manufacturing, LLC has 9 FDA 510(k) cleared medical devices. Based in Morton, US.

Latest FDA clearance: Mar 2026. Active since 2017. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Pressure Products Medical Device Manufacturing, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pressure Products Medical Device Manufacturing, LLC

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