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

ACUSON RADIOLOGY DOPPLER ACCESSORY

K Number: K852974 · Decision Oct 24, 1985
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
24
Review Days
101

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ACUSON RADIOLOGY DOPPLER ACCESSORY
K Number
K852974
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent for Some Indications
Applicant
Acuson Computed Sonography
Date Received
July 15, 1985
Decision Date
October 24, 1985
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

Similar 510(k) Clearances

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

View all

Other Clearances by Acuson Computed Sonography

K Number Device Name
K893863 ACUSON L538 TRANSDUCER
K874028 ACUSON S328 TRANSDUCER
K874861 ACUSON S328 TRANSDUCER FOR CARDIAC COLOR FLOW APP.
K874363 ACUSON S228 AND S328 TRANSDUCERS FOR ABDOM. APPLI.
K874922 ACUSON TRANSPERINEAL NEEDLE GUIDE
K874860 ACUSON I7505 TRANSDUCER FOR INTRACAVITARY APPLICA.
K871506 ACUSON L538 TRANSDUCER
K871416 AUXILIARY CONTINUOUS WAVE DOPPLER TRANSDUCER
K871239 ACUSON PHYSIOLOGICAL CONTROL MODULE
K864578 ACUSON TV519 TRANSDUCER
Search all 24 clearances from Acuson Computed Sonography →