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SMART READ BIOLOGICAL TEST PACK

K103000 Class II Special
Decision Date
2011-02-11
Sponsor / Applicant
Steritec Products Mfg Co, Inc.

Technical Specification

510(k) Submission ID K103000
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2011-02-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMART READ BIOLOGICAL TEST PACK received FDA 510(k) clearance under submission number K103000, sponsored by Steritec Products Mfg Co, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-02-11.

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.