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

ATLANTIS PV IMAGING CATHETER, MODEL 36456

K Number: K022860 · Decision Nov 21, 2002
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
19
Review Days
85

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Basic Information

Device Name
ATLANTIS PV IMAGING CATHETER, MODEL 36456
K Number
K022860
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boston Scientific, Target
Date Received
August 28, 2002
Decision Date
November 21, 2002
Product Code
ITX
Advisory Committee
Radiology
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
ITX Transducer, Ultrasonic, Diagnostic

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