# K915237: Philips PCR-Ace System

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Jan 9, 1992 after 48 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
19 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K964124: Philips Computed Radiography (1996), 18 descendants of its own
- K063781: Philips XD-S Direct Radiography Workstation/Package (2007), 16 descendants of its own
- K140771: Philips Eleva Workspot (2014), 15 descendants of its own
- K141736: Philips Prograde; Philips Eleva Workspot for Digital Diagnost (2014), 6 descendants of its own
- K203188: ADD (2021), 3 descendants of its own

Source page: https://510kreport.com/device/K915237
Methodology: https://510kreport.com/methodology