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FDA 510(k) Application Details - K060904
Device Classification Name
Catheter, Peripheral, Atherectomy
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510(K) Number
K060904
Device Name
Catheter, Peripheral, Atherectomy
Applicant
REX MEDICAL LP
55 Northern Blvd.
Suite 200
Great Neck, NY 11021 US
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Contact
SUSAN D GOLDSTEIN-FALK
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Regulation Number
870.4875
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Classification Product Code
MCW
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More FDA Info for this Product Code
Date Received
04/03/2006
Decision Date
04/28/2006
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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