# K973633: Atrion Medical Products Lacrimal Intubation Set

- Pathway: 510(k) (Traditional)
- Applicant: Atrion Medical Products, Inc.
- Decided: Jan 16, 1998 after 183 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
Longest line of descent: 1 generation back to K962151 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962151: Ryder Lacrimal Intubationset, Ryder Intl. Corp. (1996) Summary page 1.

## Indications for use
1. Maintenance of lacrimal outflow post primary DCR surgical procedures. 2. Maintenance of lacrimal outflow post failed open DCR surgical procedures with complete obstruction. 3. Reconstruction of the canaliculi.

Source page: https://510kreport.com/device/K973633
Methodology: https://510kreport.com/methodology