# K901723: MDL-2000 Lasertripter

- Pathway: 510(k) (Traditional)
- Applicant: Candela Laser Corp.
- Decided: Jul 13, 1990 after 88 days
- Product code: LNK (Laser For Gastro-Urology Use)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K023041: W.O.M. Laser U100 (2002), 1 descendant of its own
- K032023: W.O.M. Laser U100PLUS (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K901723
Methodology: https://510kreport.com/methodology