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510(k) K200094

speX LP Support Catheter by Reflow Medical — Product Code DQY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 2020
Date Received
January 16, 2020
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Percutaneous
Device Class
Class II
Regulation Number
870.1250
Review Panel
CV
Submission Type

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