PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB)

FDA 510(k) K233132 · Primus Sterilizer Company, LLC

Substantially Equivalent

510(k) numberK233132

Submission

Device name
PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB)
Applicant
Primus Sterilizer Company, LLC
Orlando, FL, US
Received
September 27, 2023
Decision date
December 19, 2023
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FLE – Sterilizer, Steam
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6880
Specialty
General Hospital

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K250168Life Ultra 25L Tabletop Mono Chamber Steam SterilizerFLE · Traditional Lucas Lifecare12/30/2025SE
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K243994Steam Sterilizer (2545D)FLE · Traditional Ningbo Ican Machines Co., Ltd.06/06/2025SE
K243801FRONT-LINE Field Sterilizer (FL135)FLE · Special Fort Defiance Industries, LLC03/07/2025SE
K233026Midmark Smart M9® Sterilizer, Midmark Smart M11® SterilizerFLE · Traditional Midmark Corporation04/04/2024SE
K233504Lexa MINI (RIS-303, RIS-305)FLE · Traditional W&H Sterilization S.R.L.02/08/2024SE
K232658T-Top 10 & T-Top T-Top 11FLE · Traditional Tuttnauer U.S.A Co, Ltd.11/27/2023SE

More from Tuttnauer U.S.A Co, Ltd.

510(k)DeviceDecision
K221474PRIMUS Healthcare Sterilizer (Model PSS11-HC)FLE · Abbreviated 02/10/2023SE
K093333Primus Steam Sterilizer PSS8-AA (16X16X26 Multi Functional Sterilizer), Lab/Lo…FLE · Abbreviated 04/02/2010SE
K082817Primus Steam Sterilizer, Models PSS5-G-1 and PSS5-MFLE · Traditional 05/21/2009SE
K991575Primus Steam SterilizersFLE · Abbreviated 12/03/1999SE
K926185Primus PSS Series SterilizersFLE · Traditional 05/09/1994SE

Questions and answers

When was PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB) cleared by the FDA?

PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB) (K233132) received a 510(k) decision of Substantially Equivalent on December 19, 2023, 83 days after the submission was received.

What is the product code of K233132?

The FDA product code is FLE – Sterilizer, Steam, a Class II (moderate risk) device regulated under 21 CFR 880.6880.