# K952049: Tru-Pulse Pulsed CO2 Surgical Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Tissue Technologies, Inc.
- Decided: Jul 21, 1995 after 81 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; 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K971830: Accu-Pulse Carbon Dioxide Laser System (1997), 1 descendant of its own
- K983543: Accu-Pulse 1000 CO2 Surgical Laser System (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K952049
Methodology: https://510kreport.com/methodology