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STERITEC DISPOSABLE BIOLOGICAL TEST PACK-EO GAS

K981497 Class II Traditional
Decision Date
1998-10-29
Sponsor / Applicant
Steritec Products Mfg Co, Inc.

Technical Specification

510(k) Submission ID K981497
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 1998-10-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERITEC DISPOSABLE BIOLOGICAL TEST PACK-EO GAS received FDA 510(k) clearance under submission number K981497, sponsored by Steritec Products Mfg Co, Inc.. 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 1998-10-29.

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.