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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Curette, Surgical, General Use
510(k) Number K831119
Device Name LUO CURRETTES #3211
Applicant
Pmt, Inc.
Box 464
Hopkins,  MN  55343
Applicant Contact Alfred A Iversen
Correspondent
Pmt, Inc.
Box 464
Hopkins,  MN  55343
Correspondent Contact Alfred A Iversen
Regulation Number878.4800
Classification Product Code
FZS  
Date Received04/05/1983
Decision Date 05/09/1983
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
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