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BEAUCOUP GENERAL PURPOSE DISINFECTANT

K960580 Class I Traditional
Decision Date
1996-03-12
Sponsor / Applicant
Huntington Laboratories, Inc.

Technical Specification

510(k) Submission ID K960580
Product Code LRJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6890
Decision Date 1996-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEAUCOUP GENERAL PURPOSE DISINFECTANT received FDA 510(k) clearance under submission number K960580, sponsored by Huntington Laboratories, 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 1996-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code LRJ and 21 CFR 880.6890, within the General Hospital review panel as a Class I device.