FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

trophon Wireless Ultrasound Probe Holder

K Number: K241536 · Decision Sep 27, 2024
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
3
Applicant Total
6
Review Days
120

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Basic Information

Device Name
trophon Wireless Ultrasound Probe Holder
K Number
K241536
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nanosonics Limited
Date Received
May 30, 2024
Decision Date
September 27, 2024
Product Code
OUJ
Advisory Committee
Radiology
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OUJ High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist

Similar 510(k) Clearances

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

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Other Clearances by Nanosonics Limited

K Number Device Name
K253267 CORIS System
DEN240018 CORIS System
K173865 trophon2
K103126 TROPHON CHEMICAL INDICATOR
K103059 TROPHON