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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Sterilant, Medical Devices
510(k) Number K932922
Device Name PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR
Applicant
Cottrell, Ltd.
7399 S. Tucson Way
Englewood,  CO  80112
Applicant Contact JACK SCOVILLE
Correspondent
Cottrell, Ltd.
7399 S. Tucson Way
Englewood,  CO  80112
Correspondent Contact JACK SCOVILLE
Regulation Number880.6885
Classification Product Code
MED  
Date Received06/15/1993
Decision Date 07/03/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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