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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Iontophoresis, Other Uses
510(k) Number K872040
Device Name PHORESOR II (TM), MODEL PM700
Applicant
Motion Control, Inc.
1290 W. 2320 S., Suite A
Salt Lake City,  UT  84119
Applicant Contact RICHARD D LUNTZ
Correspondent
Motion Control, Inc.
1290 W. 2320 S., Suite A
Salt Lake City,  UT  84119
Correspondent Contact RICHARD D LUNTZ
Regulation Number890.5525
Classification Product Code
EGJ  
Date Received05/27/1987
Decision Date 08/04/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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