# K931071: Philips Thoravision

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Sep 15, 1994 after 562 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
143 later devices descend from it; 2 cite it directly.
0 of 144 devices 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.

## Most influential descendants
- K982795: Philips Bucky Vision (1998), 141 descendants of its own
- K992794: Stingray DR, Model 1 (1999), 103 descendants of its own
- K024147: Paxscan 4030 Medical Digital Imaging System (2003), 78 descendants of its own
- K090625: Wireless Portable Detector FD-W17 (2009), 41 descendants of its own
- K092669: DX-D Imaging Package (2009), 34 descendants of its own

## Recalls of this device
- Dec 1, 2004 · Not classified · Z-0369-05: X-Ray system may fall downward and could possibly hit the patient.

Source page: https://510kreport.com/device/K931071
Methodology: https://510kreport.com/methodology