# K992864: Render-Plan 3-D

- Pathway: 510(k) (Special)
- Applicant: Precision Therapy Intl., Inc.
- Decided: Sep 9, 1999 after 15 days
- Product code: MUJ (System, Planning, Radiation Therapy Treatment)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K894722 (1990). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K894722: Renner-Plan, W.D. Renner Consulting Co. (1990). Our OCR of the scanned summary read K834722, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Render-Plan 3-D”.

## Indications for use
The Render-Plan 3-D® is intended to be used for planning the dosimetry of treatments in radiation therapy. It processes the inputs of the health care professional such that the desired radiation dose can be set on a radiation therapy delivery system.

Source page: https://510kreport.com/device/K992864
Methodology: https://510kreport.com/methodology