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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cement, Dental
510(k) Number K952121
Device Name 3M RESIN CEMENT
Applicant
3M Medical Products Group
3m Center,
Bldg. 260-2b-09
St. Paul,  MN  55144
Applicant Contact REBECCA L NANNACK
Correspondent
3M Medical Products Group
3m Center,
Bldg. 260-2b-09
St. Paul,  MN  55144
Correspondent Contact REBECCA L NANNACK
Regulation Number872.3275
Classification Product Code
EMA  
Date Received05/05/1995
Decision Date 06/22/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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