# K921219: Philips Dci-SX

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Apr 29, 1994 after 777 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
76 later devices descend from it; 2 cite it directly.
0 of 77 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
- K971965: Philips Easyvision (1998), 74 descendants of its own
- K022292: Impax Diagnostic Display Station,Impax Clinical Review Station,Impax for Cardiology Clinical Review Satation,Impax Ortho (2002), 48 descendants of its own
- K031350: 3TP Software Option (2003), 19 descendants of its own
- K041286: Dynacad V1.0 (2004), 17 descendants of its own
- K061421: Erad Pacs (2006), 14 descendants of its own

Source page: https://510kreport.com/device/K921219
Methodology: https://510kreport.com/methodology