Mevaplan and Somados
FDA 510(k) K852410 · Siemens Medical Solutions USA, Inc.
510(k) numberK852410
Submission
- Device name
- Mevaplan and Somados
- Applicant
- Siemens Medical Solutions USA, Inc.
Iselin, NJ, US - Received
- June 6, 1985
- Decision date
- October 28, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Mevaplan and Somados cleared by the FDA?
Mevaplan and Somados (K852410) received a 510(k) decision of Substantially Equivalent on October 28, 1985, 144 days after the submission was received.
What is the product code of K852410?
The FDA product code is KPQ – System, Simulation, Radiation Therapy, a Class II (moderate risk) device regulated under 21 CFR 892.5840.