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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K851651
Device Name HGM ENDOCOAGULATOR MODEL 8
Applicant
Hgm, Inc.
3959 W. 1820 S.
Salt Lake City,  UT  84104
Applicant Contact JEROME STENEHJEM
Correspondent
Hgm, Inc.
3959 W. 1820 S.
Salt Lake City,  UT  84104
Correspondent Contact JEROME STENEHJEM
Date Received04/22/1985
Decision Date 07/23/1985
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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