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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Electrical Dental Anesthesia
510(k) Number K935082
Device Name 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670 MODIFICATION
Applicant
3M Company
3m Center
Bldg. 275-3se-08
St. Paul,  MN  55144 -1000
Applicant Contact PAUL A BURGIO
Correspondent
3M Company
3m Center
Bldg. 275-3se-08
St. Paul,  MN  55144 -1000
Correspondent Contact PAUL A BURGIO
Classification Product Code
LWM  
Date Received10/22/1993
Decision Date 01/26/1994
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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