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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Sensing, Optical Contour
510(k) Number K860225
Device Name METRICOM
Applicant
Far Orthopedics, Inc.
2875 Sabourin
Montreal - Que - H4s 1m9
Canada,  CA
Applicant Contact RAAB, PH.D.
Correspondent
Far Orthopedics, Inc.
2875 Sabourin
Montreal - Que - H4s 1m9
Canada,  CA
Correspondent Contact RAAB, PH.D.
Classification Product Code
LDK  
Date Received01/22/1986
Decision Date 02/11/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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