Transducer, Ultrasonic, Diagnostic
FDA product code ITX · 410 cleared devices
Class 2
Radiology
- Regulation
- 21 CFR 892.1570
- Review panel
- RA
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1978-05-09 – 2026-09-24
ITX
1981-11-24
ITX
1981-11-16
VARIABLE FOCUS 3.5 MHZ TRANSDUCER
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ITX
1981-08-25
BIOPSY TRANSDUCER
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ITX
1981-06-19
7.5 MHZ WP TRANSDUCER
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ITX
1981-04-17
5 MHZ TRANSDUCER
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ITX
1981-01-21
MARK V DUPLEX ULTRASONIC SCAN SYS.
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ITX
1980-10-23
IN-LINE SCAN HEAD MARK IV DUPLEX ULTRA
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ITX
1980-10-23
IN-LINE SCAN HEAD MODIFICATION MARK III
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ITX
1978-12-07
ULTRASONIC TRANSDUCERS
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ITX
1978-05-09
ULTRASONIC DIAGNOSTIC TRANSDUCER
View details →No matching devices.
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