# K993947: Koordinant Angiographic and Operating Room Model X-Ray Table Family

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Corp.
- Decided: Dec 21, 1999 after 29 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K883613 (1988). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K951176: Koordinat M, Siemens Medical Solutions USA, Inc. (1995) Summary page 1.
- K883613: Oper. Table for Percutan. Trans. Coronary Angio., Stierlen-Maquet AG (1988) Summary page 1.
- K940696: Syncra Tilt Option for Angio Diagnost 5, Philips Medical Systems North America, Inc. (1994) Summary page 1.
- K884531: Beta 90/50 Mobile Imaging Table, Beta Medical Products Co. (1989) Summary page 1.

## Indications for use
The Siemens Koordinat Angiographic X-ray Table family is intended to support and position patients for Angiographic examinations, Angiographic interventional techniques where an X-ray translucent tabletop is required, and for use during surgery where an X-ray translucent tabletop is required.

Source page: https://510kreport.com/device/K993947
Methodology: https://510kreport.com/methodology