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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Sterilizer, Dry Heat
510(k) Number K910925
Device Name DISINFECTION WITH THE COX DRY HEAT STERILIZER
Applicant
Cox Sterile Products, Inc.
5115 Mckinney Ave., Suite C
Dallas,  TX  75205
Applicant Contact KEITH COX
Correspondent
Cox Sterile Products, Inc.
5115 Mckinney Ave., Suite C
Dallas,  TX  75205
Correspondent Contact KEITH COX
Regulation Number880.6870
Classification Product Code
KMH  
Date Received03/05/1991
Decision Date 05/08/1992
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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