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

IREX PS, PORTABLE SCANNER AND 118

K Number: K844404 · Decision Feb 4, 1985
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
10
Review Days
83

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Basic Information

Device Name
IREX PS, PORTABLE SCANNER AND 118
K Number
K844404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Irex Corp.
Date Received
November 13, 1984
Decision Date
February 4, 1985
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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K Number Device Name
K843643 COLOR DOPPLER 880
K842408 IREX 730 MECHANICAL SECTOR SCANNER
K840139 IREX 720 SECTOR SCANNER
K827370 IREX SYSTEM II 2D/DOPPLER IMAGING SYSTEM
K813544 IREX 2D/DOPPLER PHASE ARRAY IMAGING SYS.
K811246 DOPPLER ULTRASOUND BLOOD FLOWMETER
K792525 IREX CARDIOPLAN
K791317 IREX REAL TIME PHASED ARRAY SYSTEM
K771372 SYSTEM II