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FDA 510(k) Application Details - K050926
Device Classification Name
Device, Percutaneous Retrieval
More FDA Info for this Device
510(K) Number
K050926
Device Name
Device, Percutaneous Retrieval
Applicant
IDEV TECHNOLOGIES, INC.
1110 NASA RD. ONE
SUITE 311
HOUSTON, TX 77058-3345 US
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Contact
SHANNON HURD
Other 510(k) Applications for this Contact
Regulation Number
870.5150
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Classification Product Code
MMX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/13/2005
Decision Date
05/09/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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