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

ULTRA IMAGER 2000

K Number: K834282 · Decision Apr 23, 1984
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
69
Review Days
154

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Basic Information

Device Name
ULTRA IMAGER 2000
K Number
K834282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Honeywell, Inc.
Date Received
November 21, 1983
Decision Date
April 23, 1984
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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