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

BIFOCAL 3.0MHZ

K Number: K833224 · Decision Nov 29, 1983
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
10
Review Days
84

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Basic Information

Device Name
BIFOCAL 3.0MHZ
K Number
K833224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Adr Ultrasound
Date Received
September 6, 1983
Decision Date
November 29, 1983
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.

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Other Clearances by Adr Ultrasound

K Number Device Name
K840408 LINEAR ARRAY TRANSDUCER OR SCANHEAD
K834141 ULTRASOUND SCAN HEAD 3.5 MHZ
K828049 ADR ULTRASOUND MC2 LARGE CART
K828051 ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC
K828053 ADR ULTRASOUND 5.5 MHZ SHORT FOCUS TRANSDUCER
K828050 ADR ULTRASOUND MODEL 4000 L
K813543 ADR ULTRASOUND MODELS 4000S & 4000S/L
K812301 VARIABLE FOCUS 3.5 MHZ TRANSDUCER
K792446 ADR REAL-TIME SECTOR SCANNER