# K951775: Ceralas Diode Laser System (Model Ceralas D50)

- Pathway: 510(k) (Traditional)
- Applicant: Ceram Optec, Inc.
- Decided: Jul 17, 1995 after 91 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.
300 later devices descend from it; 4 cite it directly.
0 of 301 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
- K050738: FT Fiber Optic Delivery Systems (2005), 225 descendants of its own
- K060033: Profile Multi-Platform System (2006), 221 descendants of its own
- K983058: Ceralas D Laser System, Model # Ceralas D15 (1998), 208 descendants of its own
- K991891: Ceralas Diode Laser System, Model Ceralas D15 (1999), 207 descendants of its own
- K073063: 15W Ceralas D 1470NM Diode Laser (2008), 202 descendants of its own

Source page: https://510kreport.com/device/K951775
Methodology: https://510kreport.com/methodology