RayStation

System, Planning, Radiation Therapy Treatment

RaySearch Laboratories AB (publ)

The following data is part of a premarket notification filed by Raysearch Laboratories Ab (publ) with the FDA for Raystation.

Pre-market Notification Details

• Device ID: K171536
• 510k Number: K171536
• Device Name: RayStation
• Classification: System, Planning, Radiation Therapy Treatment
• Applicant: RaySearch Laboratories AB (publ) Sveav 44 Stockholm, SE 111 34
• Contact: David Hedfors
• Correspondent: David Hedfors; RaySearch Laboratories AB (publ) Sveav 44 Stockholm, SE 111 34
• Product Code: MUJ
• CFR Regulation Number: 892.5050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2017-05-25
• Decision Date: 2017-06-27
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
07350002010075	K171536	000
07350002010037	K171536	000