# K990672: Lacrimal Intubation Set, Dacryocystorhinostomy (DCR) Set

- Pathway: 510(k) (Traditional)
- Applicant: Hurricane Medical
- Decided: May 18, 1999 after 77 days
- Product code: OKS (Lacrimal Stents And Intubation Sets)
- Device class: U
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) Lacrimal Intubation Set manufactured and distributed by JEDMED: named in the summary without a submission number
- (no number) Canaliculus Intubation Set manufactured and distributed by SOLAN: named in the summary without a submission number
- (no number) Lacrimal Intubation Set and DCR Set manufactured and distributed by VISITEC: named in the summary without a submission number

## Most influential descendants
- K030353: Monocanalicular Stents, Lacrimal Intubation Sets (2003), 2 descendants of its own
- K113316: DCS Lacrimal Stent (2012), 1 descendant of its own
- K140290: Stoploss Jones Tube (2014), 0 descendants of its own

## Indications for use
These devices are used in ophthalmic surgery to reconstruct the lacrimal outflow system, dacryocystorhinostomy, and other lacrimal system reconstruction.

Source page: https://510kreport.com/device/K990672
Methodology: https://510kreport.com/methodology