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FDA 510(k) Application Details - K953850
Device Classification Name
Sleeve, Limb, Compressible
More FDA Info for this Device
510(K) Number
K953850
Device Name
Sleeve, Limb, Compressible
Applicant
KINETIC CONCEPTS, INC.
P.O. BOX 659508
SAN ANTONIO, TX 78216-9508 US
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Contact
WILLIAM H QUIRK
Other 510(k) Applications for this Contact
Regulation Number
870.5800
More FDA Info for this Regulation Number
Classification Product Code
JOW
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More FDA Info for this Product Code
Date Received
08/16/1995
Decision Date
03/04/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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