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

COLOR FLOW IMAGING

K Number: K873096 · Decision Nov 23, 1987
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
61
Review Days
108

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Basic Information

Device Name
COLOR FLOW IMAGING
K Number
K873096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Advanced Technology Laboratories, Inc.
Date Received
August 7, 1987
Decision Date
November 23, 1987
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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K992470 ULTRAMARK 400C/SONOACE 6000 ULTRASOUND SYSTEM
K991671 HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM
K961459 LEVEL 10 HDI
K935009 PEGASUS
K940423 NOVA MICROSONICS ACCESS IMAGE MANAGEMENT NETWORK/ACCESS ACQUISITION MODULE
K905248 NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS
K903603 ULTRAMARK 9 ULTRASOUND SYSTEM (UM 9)
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