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FDA 510(k) Application Details - K030714
Device Classification Name
System, Optical Position/Movement Recording
More FDA Info for this Device
510(K) Number
K030714
Device Name
System, Optical Position/Movement Recording
Applicant
PEAK PERFORMANCE TECHNOLOGIES, INC
7388 S. REVERE PKY 901
CENTINNIAL, CO 80112 US
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Contact
LARRY SCHEIRMAN
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LXJ
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More FDA Info for this Product Code
Date Received
03/06/2003
Decision Date
05/16/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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