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

PUREIMAGE ULTRASOUND TRANSMISSION GEL

K Number: K120156 · Decision Feb 8, 2012
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
11
Review Days
21

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Basic Information

Device Name
PUREIMAGE ULTRASOUND TRANSMISSION GEL
K Number
K120156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medline
Date Received
January 18, 2012
Decision Date
February 8, 2012
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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