Atlas FDA

cmTriage

FDA 510(k) clearance K183285 · decided 2019-03-08

Clearance details

K-number
K183285
Device name
cmTriage
Applicant
Curemetrix, Inc.
Decision
Substantially Equivalent
Date received
2018-11-26
Decision date
2019-03-08
Days to decision
102 days
Clearance type
Traditional
Product code
QFM
Device class
2
Regulation number
892.2080
Medical specialty
Radiology
Advisory committee
Radiology
Location
La Jolla, CA, US
Third-party review
No
Expedited review
No

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VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage (K241439)Vuno, Inc.2024-11-15
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VinDr-Mammo (K233108)Vinbigdata Joint Stock Company2024-05-23
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Recalls involving this device

No recalls on record reference this clearance.