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

MARK V DUPLEX ULTRASONIC SCAN SYS.

K Number: K802438 · Decision Jan 21, 1981
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
61
Review Days
107

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Basic Information

Device Name
MARK V DUPLEX ULTRASONIC SCAN SYS.
K Number
K802438
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Advanced Technology Laboratories, Inc.
Date Received
October 6, 1980
Decision Date
January 21, 1981
Product Code
ITX
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
ITX Transducer, Ultrasonic, Diagnostic

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