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

SACA, 3.5 MHZ PROBE

K Number: K905200 · Decision Apr 2, 1992
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
42
Review Days
499

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Basic Information

Device Name
SACA, 3.5 MHZ PROBE
K Number
K905200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Diasonics, Inc.
Date Received
November 20, 1990
Decision Date
April 2, 1992
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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Other Clearances by Diasonics, Inc.

K Number Device Name
K962662 VINGMED SOUND COLOR FLOW MAPPING SYSTEM
K924079 CFM-800 COLOR FLOW MAPPING SYSTEM
K911435 CPA/3.5 MHZ PROBE
K903562 CW DOPPLER 2.25 MHZ PROBE
K903984 CW DOPPLER/4.5 MHZ
K896637 ACCESS(TM), SOFTWARE RELEASE 4.11P
K893518 MT/S SOFTWARE RELEASE 5.0.
K894290 ACCESS TM
K893881 ACCESS TM
K891452 SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE
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