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FDA 510(k) Application Details - K001909
Device Classification Name
Wheelchair, Mechanical
More FDA Info for this Device
510(K) Number
K001909
Device Name
Wheelchair, Mechanical
Applicant
PLAINSENSE WHEELCHAIRS, INC.
2919 BENTWOOD DR.
MARIETTA, GA 30062-4608 US
Other 510(k) Applications for this Company
Regulation Number
890.3850
More FDA Info for this Regulation Number
Classification Product Code
IOR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/22/2000
Decision Date
08/25/2000
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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