# K191026: Medip Pro

- Pathway: 510(k) (Traditional)
- Applicant: Medical IP Co., Ltd.
- Decided: Nov 7, 2019 after 203 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K924630 (1993). 6 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173619: Mimics inPrint, Materialise NV (2018) Summary page 5.

## Most influential descendants
- K223556: DeepCatch (2023), 1 descendant of its own
- K253944: Data Analysis Facilitation Suite (DAFS) (2026), 0 descendants of its own

## Indications for use
MEDIP PRO is intended for use as a software interface and image segmentation system for the transfer of DICOM imaging information from a medical scanner to an output file. It is also used as pre-operative software for treatment planning. The 3D printed models generated from the output file are meant for non-diagnostic use. MEDIP PRO should be used in conjunction with other diagnostic tools and expert clinical judgement.

Source page: https://510kreport.com/device/K191026
Methodology: https://510kreport.com/methodology