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

VINGMED SOUND COLOR FLOW MAPPING SYSTEM

K Number: K962662 · Decision Jan 2, 1997
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
42
Review Days
178

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Basic Information

Device Name
VINGMED SOUND COLOR FLOW MAPPING SYSTEM
K Number
K962662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diasonics, Inc.
Date Received
July 8, 1996
Decision Date
January 2, 1997
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IYO), ordered by most recent decision date.

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Other Clearances by Diasonics, Inc.

K Number Device Name
K924079 CFM-800 COLOR FLOW MAPPING SYSTEM
K911435 CPA/3.5 MHZ PROBE
K905200 SACA, 3.5 MHZ PROBE
K903562 CW DOPPLER 2.25 MHZ PROBE
K903984 CW DOPPLER/4.5 MHZ
K896637 ACCESS(TM), SOFTWARE RELEASE 4.11P
K893518 MT/S SOFTWARE RELEASE 5.0.
K894290 ACCESS TM
K893881 ACCESS TM
K891452 SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE
Search all 42 clearances from Diasonics, Inc. →