Atlas FDA

Solas OR

FDA 510(k) clearance K213691 · decided 2021-12-22

Clearance details

K-number
K213691
Device name
Solas OR
Applicant
Cirdan Imaging, Ltd.
Decision
Substantially Equivalent
Date received
2021-11-23
Decision date
2021-12-22
Days to decision
29 days
Clearance type
Traditional
Product code
MWP
Device class
2
Regulation number
892.1680
Medical specialty
Radiology
Advisory committee
Radiology
Location
Lisburn, GB
Third-party review
Yes
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.