Atlas FDA

trophon2

FDA 510(k) clearance K250434 · decided 2025-08-05

Clearance details

K-number
K250434
Device name
trophon2
Applicant
Nanosonics
Decision
Substantially Equivalent
Date received
2025-02-14
Decision date
2025-08-05
Days to decision
172 days
Clearance type
Traditional
Product code
OUJ
Device class
2
Regulation number
892.1570
Medical specialty
Radiology
Advisory committee
Radiology
Location
Macquarie Park, AU
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
trophon Wireless Ultrasound Probe Holder (K241536)Nanosonics Limited2024-09-27
trophon2 (K173865)Nanosonics Limited2018-04-24
TROPHON (K103059)Nanosonics Limited2011-02-24

Recalls involving this device

No recalls on record reference this clearance.