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FDA 510(k) Application Details - K993298
Device Classification Name
Wheelchair, Mechanical
More FDA Info for this Device
510(K) Number
K993298
Device Name
Wheelchair, Mechanical
Applicant
PREMIER DESIGNS
4834 W. JACQUELYN, SUITE 101
FRESNO, CA 93722 US
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Contact
CHRIS BERRYHILL
Other 510(k) Applications for this Contact
Regulation Number
890.3850
More FDA Info for this Regulation Number
Classification Product Code
IOR
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More FDA Info for this Product Code
Date Received
10/01/1999
Decision Date
11/16/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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