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STERRAAD 100NX EXPRESS CYCLE TEST PACK

K092755 Class II Traditional
Decision Date
2011-02-25
Sponsor / Applicant
Advanced Sterilization Products

Technical Specification

510(k) Submission ID K092755
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2011-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERRAAD 100NX EXPRESS CYCLE TEST PACK received FDA 510(k) clearance under submission number K092755, sponsored by Advanced Sterilization Products. 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 2011-02-25.

Classification & Regulation

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