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FDA 510(k) Application Details - K213664
Device Classification Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
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510(K) Number
K213664
Device Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant
B. Braun Medical Inc.
901 Marcon Blvd.
Allentown, PA 18109 US
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Contact
Tracy Larish
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Regulation Number
880.5200
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Classification Product Code
FOZ
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More FDA Info for this Product Code
Date Received
11/22/2021
Decision Date
02/11/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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