Radiation Treatment Planning System
FDA 510(k) K780157 · Capintec, Inc.
510(k) numberK780157
Submission
- Device name
- Radiation Treatment Planning System
- Applicant
- Capintec, Inc.
Mchenry, IL, US - Received
- January 30, 1978
- Decision date
- February 13, 1978
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Radiation Treatment Planning System cleared by the FDA?
Radiation Treatment Planning System (K780157) received a 510(k) decision of Substantially Equivalent on February 13, 1978, 14 days after the submission was received.
What is the product code of K780157?
The FDA product code is JAD – System, Therapeutic, X-Ray, a Class II (moderate risk) device regulated under 21 CFR 892.5900.