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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K833364
Device Name 3M SCOTCHPLATE II DISPERSIVE ELECTRODE
Applicant
3M Company
2724 S. Peck Rd.
Monrovia,  CA  91016
Correspondent
3M Company
2724 S. Peck Rd.
Monrovia,  CA  91016
Regulation Number878.4400
Classification Product Code
GEI  
Date Received09/28/1983
Decision Date 11/29/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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