# K842810: Infrared Coagulator

- Pathway: 510(k) (Traditional)
- Applicant: Endo Lase, Inc.
- Decided: Oct 18, 1984 after 92 days
- Product code: KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories))
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
110 later devices descend from it; 1 cites it directly.
0 of 111 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
- K974168: Coopersurgical Infrared Coagulator (1998), 109 descendants of its own
- K060069: Palomar Luxir Fractional Handpiece (2006), 107 descendants of its own
- K070298: Modification to Palomar Luxir Handpiece (2007), 64 descendants of its own
- K110907: Palomar Icon (TM) Aesthetic System (2011), 57 descendants of its own
- K111303: Dermatological Treatment Device Family (2011), 56 descendants of its own

Source page: https://510kreport.com/device/K842810
Methodology: https://510kreport.com/methodology