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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pad, Kelly
510(k) Number K831117
Device Name MICROMAT W/VARIOUS MODELS
Applicant
Pmt, Inc.
Box 464
Hopkins,  MN  55343
Applicant Contact Carroll E Reynolds
Correspondent
Pmt, Inc.
Box 464
Hopkins,  MN  55343
Correspondent Contact Carroll E Reynolds
Regulation Number878.4370
Classification Product Code
FNW  
Subsequent Product Code
KKX  
Date Received04/05/1983
Decision Date 05/30/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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