FDA 510(k) Application Details - K874300

Device Classification Name Discriminator,Two-Point

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510(K) Number K874300
Device Name Discriminator,Two-Point
Applicant ORTHOPEDIC SYSTEMS, INC.
1897 NATIONAL AVE.
HAYWARD, CA US
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Contact ROBERTY R MOORE
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Regulation Number 882.1200

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Classification Product Code GWI
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Date Received 10/20/1987
Decision Date 11/06/1987
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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