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

DOPSCAN PLUS DS1060

K Number: K843891 · Decision Jan 9, 1985
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
11
Review Days
99

Basic Information

Device Name
DOPSCAN PLUS DS1060
K Number
K843891
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
CAROLINA MEDICAL ELECTRONICS
Date Received
October 2, 1984
Decision Date
January 9, 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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