Atlas FDA

RefleXion Medical Radiotherapy System (RMRS)

FDA 510(k) clearance DEN220014 · decided 2023-02-01

Clearance details

K-number
DEN220014
Device name
RefleXion Medical Radiotherapy System (RMRS)
Applicant
Reflexion Medical, Inc.
Decision
Unknown
Date received
2022-02-23
Decision date
2023-02-01
Days to decision
343 days
Clearance type
Direct
Product code
QVA
Device class
2
Regulation number
892.5060
Medical specialty
Radiology
Advisory committee
Radiology
Location
Hayward, CA, US
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
RefleXion Medical Radiotherapy System, Reflexion X2 (K252071)Reflexion Medical, Inc.2025-12-18

Recalls involving this device

No recalls on record reference this clearance.