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FDA 510(k) Application Details - K081940
Device Classification Name
Dilator, Vessel, For Percutaneous Catheterization
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510(K) Number
K081940
Device Name
Dilator, Vessel, For Percutaneous Catheterization
Applicant
AVALON LABORATORIES, LLC
2610 E. HOMESTEAD PLACE
RANCHO DOMINGUEZ, CA 90220 US
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Contact
LEE WIRTH
Other 510(k) Applications for this Contact
Regulation Number
870.1310
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Classification Product Code
DRE
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More FDA Info for this Product Code
Date Received
07/08/2008
Decision Date
11/18/2008
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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