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FDA 510(k) Application Details - K970669
Device Classification Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
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510(K) Number
K970669
Device Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant
AEROQUIP MEDICAL PRODUCTS
2323 GREEN RD.
ANN ARBOR, MI 48105 US
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Contact
CHRISTINA L THOMAS
Other 510(k) Applications for this Contact
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
02/24/1997
Decision Date
08/01/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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