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FDA 510(k) Application Details - K201288
Device Classification Name
Dilator, Vessel, For Percutaneous Catheterization
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510(K) Number
K201288
Device Name
Dilator, Vessel, For Percutaneous Catheterization
Applicant
Baylis Medical Company Inc.
2580 Matheson Blvd. East
Mississauga L4W 4J1 CA
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Contact
May Tsai
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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
05/14/2020
Decision Date
06/12/2020
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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