# K180765: Televere Podiatry X-Ray System HF

- Pathway: 510(k) (Traditional)
- Applicant: Televere Systems, Inc.
- Decided: Apr 20, 2018 after 28 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K981556 (1998). 23 ancestors in all.
No later device cites it as a predicate yet.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160857: HF 718BD X-Ray System, Arquilla, Inc. Dba X-Cel X-Ray Corporation (2017) Summary page 4.
- K170975: Televere Digital Imaging System, Televere Systems (2017) Summary page 6.

## Indications for use
The Televere Podiatry X-Ray System HF is intended for use by qualified clinicians for the x-ray of hands and feet. Not for mammography. Not fluoroscopy.

Source page: https://510kreport.com/device/K180765
Methodology: https://510kreport.com/methodology