# K113536: Masterka 40 Masterka 35 Masterka 30

- Pathway: 510(k) (Traditional)
- Applicant: Fci Sas (France Chirurgie Instrumentation)
- Decided: Aug 3, 2012 after 247 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 K061404 (2006). 1 ancestor in all.
1 later device descends 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)
- K061404: Mono-Crawford Naso-Lacrimal Intubation Device, Fci Ophthalmics, Inc. (2006) Summary page 1.

## Most influential descendants
- K201606: LacriJet® (2020), 0 descendants of its own

## Indications for use
The MASTERKA®0 is a silicone intubation device indicated for use in the treatment of congenital lacrimal duct obstructions (stenosis of the valve of Hasner) in patients 12 months and older.

Source page: https://510kreport.com/device/K113536
Methodology: https://510kreport.com/methodology