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STEAMPLUS STERILIZATION TEST

K020409 Class II Traditional
Decision Date
2002-07-18
Sponsor / Applicant
Spsmedical Supply Corp.

Technical Specification

510(k) Submission ID K020409
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2002-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STEAMPLUS STERILIZATION TEST received FDA 510(k) clearance under submission number K020409, sponsored by Spsmedical Supply Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2002-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.