FDA 510(k), K223209, Elekta Unity
FDA 510(k), K223209, Elekta Unity
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$149.00 USD
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510(K) Number: K223209
Device Name: Elekta Unity
Manufacturer: Melinda Smith
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 10/17/2022
Date Received: 02/23/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: Elekta Unity
Manufacturer: Melinda Smith
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 10/17/2022
Date Received: 02/23/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology