FDA 510(k), K203722, RayPilot System
FDA 510(k), K203722, RayPilot System
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$149.00 USD
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510(K) Number: K203722
Device Name: RayPilot System
Manufacturer: Thomas Lindstrom
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 12/21/2020
Date Received: 09/02/2021
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: RayPilot System
Manufacturer: Thomas Lindstrom
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 12/21/2020
Date Received: 09/02/2021
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology