# K860087: Sharplan Model 1020 CO2 Surgical Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Sharplan Lasers, Inc.
- Decided: Apr 24, 1986 after 105 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K980398: Kaplan Pendulaser 115 Surgical Laser with Optoscan II (1998), 0 descendants of its own
- K971821: Unica 315 M CO2 Surgical Laser System (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K860087
Methodology: https://510kreport.com/methodology