Primus Sterilizer Company, LLC is one of 16144 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Primus Sterilizer Company, LLC - FDA 510(k) Cleared Devices
Recent clearances: PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB), PRIMUS Healthcare Sterilizer (Model PSS11-HC), PRIMUS STEAM STERILIZER PSS8-AA (16X16X26 MULTI FUNCTIONAL STERILIZER), LAB/LO STERILIZER,PRIMUS STEAM STERILIZER PSS8
4
Total
4
Cleared
0
Denied
Primus Sterilizer Company, LLC has 4 FDA 510(k) cleared medical devices. Based in Great Bend, US.
Last cleared in 2023. Active since 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Primus Sterilizer Company, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by IZiel Healthcare and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Primus Sterilizer Company, LLC
4 devices
Cleared
Dec 19, 2023
PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB)
General Hospital
83d
Cleared
Feb 10, 2023
PRIMUS Healthcare Sterilizer (Model PSS11-HC)
General Hospital
266d
Cleared
Apr 02, 2010
PRIMUS STEAM STERILIZER PSS8-AA (16X16X26 MULTI FUNCTIONAL STERILIZER),...
General Hospital
158d
Cleared
May 21, 2009
PRIMUS STEAM STERILIZER, MODELS PSS5-G-1 AND PSS5-M
General Hospital
238d