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

SONOS IMAGING SYSTEM (2000/2500 & 1000/1500)

K Number: K952540 · Decision Mar 11, 1996
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
230
Review Days
293

Basic Information

Device Name
SONOS IMAGING SYSTEM (2000/2500 & 1000/1500)
K Number
K952540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HEWLETT-PACKARD CO.
Date Received
May 23, 1995
Decision Date
March 11, 1996
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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