# K790688: Mevatron 67

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Laboratories, Inc.
- Decided: Apr 23, 1979 after 13 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

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

## Recalls of this device
- Jan 25, 2017 · Class II · Z-1433-2017: Siemens became aware of a defective weld seam at overhead suspensions. Due to this defect it is possible for the weld seam to break and to cause the overhead suspension to fall down. This can lead to 
- May 28, 2014 · Class II · Z-2174-2014: A safety risk exists with automatically sequenced treatment technique using the SIMTEC Auto Field Option where automatic movements of the gantry and the tabletop during an auto-sequenced treatment hav

Source page: https://510kreport.com/device/K790688
Methodology: https://510kreport.com/methodology