Pressure Products Medical Device Manufacturing, LLC
Pressure Products Medical Device Manufacturing, LLC holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2026.
Top product codes for Pressure Products Medical Device Manufacturing, LLC
Recent clearances by Pressure Products Medical Device Manufacturing, LLC
- K253799 — SafeSept RF Transseptal Guidewire (SSRF132; SSRF132R; SSRF232; SSRF232R; SSRF135; SSRF135R; SSRF235; SSRF235R)
- K241042 — SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198)
- K221707 — SafeSept® Transseptal Guidewire (SS-140)
- K210328 — SafeSept Blunt Needle
- K181031 — TSI Transseptal Introducer
- K172950 — TSN Transseptal Needle
- K172934 — Needle Free Transseptal Cannula
- K172893 — SafeSept Needle Free Transseptal Guidewire
- K170671 — SafeSept Transseptal Guidewire
Data sourced from openFDA. This site is unofficial and independent of the FDA.