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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Indicator, Physical/Chemical Sterilization Process
510(k) Number K193254
FOIA Releasable 510(k) K193254
Device Name 3M Attest Steam Chemical Integrator
Applicant
3M Company
3M Center, Building 275-5W-06
St. Paul,  MN  55144
Applicant Contact Mary Fretland
Correspondent
3M Company
3M Center, Building 275-5W-06
St. Paul,  MN  55144
Correspondent Contact Mary Fretland
Regulation Number880.2800
Classification Product Code
JOJ  
Date Received11/26/2019
Decision Date 12/23/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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