FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EMBOLECTOMY/THROMBECTOMY BALLOON CATHETER

K Number: K864007 · Decision Jan 2, 1987
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
45
Review Days
79

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Basic Information

Device Name
EMBOLECTOMY/THROMBECTOMY BALLOON CATHETER
K Number
K864007
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Uresil Corp.
Date Received
October 15, 1986
Decision Date
January 2, 1987
Product Code
DXE
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXE Catheter, Embolectomy

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K953923 URESIL INTRODUCING NEEDLE
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