# K883613: Oper. Table for Percutan. Trans. Coronary Angio.

- Pathway: 510(k) (Traditional)
- Applicant: Stierlen-Maquet AG
- Decided: Sep 15, 1988 after 24 days
- Product code: GDC (Table, Operating-Room, Electrical)
- Device class: 1
- Regulation: 21 CFR 878.4960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K993947: Koordinant Angiographic and Operating Room Model X-Ray Table Family (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K883613
Methodology: https://510kreport.com/methodology