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PRIMUS Healthcare Sterilizer (Model PSS11-HC)

K221474 Class II Abbreviated
Decision Date
2023-02-10
Sponsor / Applicant
Primus Sterilizer Company, LLC

Technical Specification

510(k) Submission ID K221474
Product Code FLE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6880
Decision Date 2023-02-10
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIMUS Healthcare Sterilizer (Model PSS11-HC) received FDA 510(k) clearance under submission number K221474, sponsored by Primus Sterilizer Company, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2023-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code FLE and 21 CFR 880.6880, within the General Hospital review panel as a Class II device.