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

SONOSITE MAXX SERIES ULTRASOUND SYSTEM

K Number: K082098 · Decision Aug 25, 2008
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
23
Review Days
31

Basic Information

Device Name
SONOSITE MAXX SERIES ULTRASOUND SYSTEM
K Number
K082098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SONOSITE,INC.
Date Received
July 25, 2008
Decision Date
August 25, 2008
Product Code
IYN
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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