# K924593: Diagnost 76 Family*R/F Systems - Release 4.4

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Nov 24, 1992 after 75 days
- Product code: IXL (Device, Spot-Film)
- Device class: 2
- Regulation: 21 CFR 892.1670
- 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.
8 later devices descend from it; 1 cites it directly.
0 of 9 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
- K970640: Philips Easy Diagnost (1997), 7 descendants of its own
- K031535: Philips Easydiagnost Eleva (2003), 6 descendants of its own
- K173433: ProxiDiagnost N90 (2018), 2 descendants of its own
- K163210: Philips CombiDiagnost R90 (2017), 2 descendants of its own
- K212837: ProxiDiagnost N90 (2021), 1 descendant of its own

## Recalls of this device
- Jan 4, 2008 · Not classified · Z-2404-2010: Potential for the tower (holding the serial changer and/or image intensifier) to slide unexpectedly and potentially injure a patient or user in its path.

Source page: https://510kreport.com/device/K924593
Methodology: https://510kreport.com/methodology