# K935412: Med-Tec, Inc. Breast Board, MT-200

- Pathway: 510(k) (Traditional)
- Applicant: Medtec, Inc.
- Decided: Jul 18, 1994 after 251 days
- Product code: IYE (Accelerator, Linear, Medical)
- 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
No predicates in its family tree.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K040773: Pelvis Bellyboard Plus Patient Positioning System (2004), 9 descendants of its own
- K122888: CDR Systems Precision Patient Positioning System (2013), 5 descendants of its own
- K153026: Body Pro-Lok Respiratory Plate, Respiratory Plate Cushion, Body Pro-Respiratory Belt, Rail Clamp for Respiratory Belt, Pressure Gauge Replacement (2016), 3 descendants of its own
- K210894: Siddharth-II; Impact (2021), 1 descendant of its own
- K132124: Klarity Vacuum Bag, Klarity Mold Cushion (2013), 1 descendant of its own

Source page: https://510kreport.com/device/K935412
Methodology: https://510kreport.com/methodology