# K882613: Alm Surgical Lamps

- Pathway: 510(k) (Traditional)
- Applicant: Alm Surgical Equipment, Inc.
- Decided: Jul 18, 1988 after 24 days
- Product code: FTD (Lamp, Surgical)
- Device class: 2
- Regulation: 21 CFR 878.4580
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K982063: Alm Prismalix (PRX) Surgical Light (1998), 2 descendants of its own
- K040015: Modification to Prismalix Surgical Light (2004), 0 descendants of its own
- K030906: Axcel Surgical Light (2003), 0 descendants of its own

## Recalls of this device
- Feb 23, 2009 · Not classified · Z-1153-2009: The screws holding the Prismatic triple surgical lights may break due to dynamic multidirectional bending stress. The firm has received one complaint report.
- Feb 23, 2009 · Not classified · Z-1154-2009: The screws holding the Prismatic triple surgical lights may break due to dynamic multidirectional bending stress. The firm has received one complaint report.

Source page: https://510kreport.com/device/K882613
Methodology: https://510kreport.com/methodology