# K181177: Interventional Workspot

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: May 31, 2018 after 29 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
Longest line of descent: 10 generations back to K890348 (1989). 53 ancestors in all.
No later device cites it as a predicate yet.
0 of 54 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121296: Interventional Workspot, Philips Medical Systems Nederland B.V. (2013) Summary page 4.

## Indications for use
The Interventional Workspot has the following medical purpose: • import, export and storage of digital clinical images, • manage the patient information associated with those images. Patient Population: Not applicable because Interventional Workspot is only a hosting platform. Operating Profile: The operator of the Interventional Workspot has basic understanding of the operating principle of medical computer software. Clinical Environment: The software can be used in the control room and in the exam room of an interventional suite and/or operating room.

Source page: https://510kreport.com/device/K181177
Methodology: https://510kreport.com/methodology