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FDA 510(k) Application Details - K080506
Device Classification Name
Wheelchair, Mechanical
More FDA Info for this Device
510(K) Number
K080506
Device Name
Wheelchair, Mechanical
Applicant
MARTIN MANUFACTURING CO., LLC
621-101 HUTTON ST
RALEIGH, NC 27606 US
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Contact
MICHAEL ZAPATA, III
Other 510(k) Applications for this Contact
Regulation Number
890.3850
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Classification Product Code
IOR
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More FDA Info for this Product Code
Date Received
02/25/2008
Decision Date
06/09/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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