# K823536: Intralig

- Pathway: 510(k) (Traditional)
- Applicant: Miltex Instrument Co.
- Decided: Dec 28, 1982 after 28 days
- Product code: EJI (Syringe, Cartridge)
- Device class: 2
- Regulation: 21 CFR 872.6770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K991888: Miniject (1999), 4 descendants of its own
- K040671: Eroject, Miniject, Self Aspirating Syringes, Aspirating Syringes, Non Aspirating Syringes (2004), 3 descendants of its own
- K083796: Miltex Aspirating Syringe, Miltex Petite Aspirating Syringe, Miltex Self-Aspirating Syringe, Miltex Lightweight (2009), 2 descendants of its own
- K171254: LeEject 2 Dental Syringe and Needle System (2017), 0 descendants of its own
- K142414: Miltex N-Tralig Intraligamentary Syringe (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K823536
Methodology: https://510kreport.com/methodology