# K954467: Cadplan BT

- Pathway: 510(k) (Traditional)
- Applicant: Varian Assoc., Inc.
- Decided: Mar 15, 1996 after 171 days
- Product code: JAQ (System, Applicator, Radionuclide, Remote-Controlled)
- Device class: 2
- Regulation: 21 CFR 892.5700
- 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 K945383 (1995). 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)
- K945383: High Dose Rate Afterloader, Varian Assoc., Inc. (1995) Summary page 1.

## Indications for use
CADPLAN BT is designed to allow the dose distribution of an applicator to be individually shaped for each patient.

Source page: https://510kreport.com/device/K954467
Methodology: https://510kreport.com/methodology