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

EAGLE EYE PLATINUM DIGITAL IVUS CATHETER

K Number: K092596 · Decision Dec 10, 2009
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
72
Applicant Total
38
Review Days
108

Basic Information

Device Name
EAGLE EYE PLATINUM DIGITAL IVUS CATHETER
K Number
K092596
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.1200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VOLCANO CORPORATION
Date Received
August 24, 2009
Decision Date
December 10, 2009
Product Code
OBJ
Advisory Committee
Cardiovascular
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
OBJ Catheter, Ultrasound, Intravascular

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