# K913136: Laser Endoscope Disc Decompression Kits

- Pathway: 510(k) (Traditional)
- Applicant: Medical Laser, Inc.
- Decided: Nov 1, 1991 after 108 days
- Product code: LRO (General Surgery Tray)
- Device class: 2
- Regulation: 21 CFR 878.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
484 later devices descend from it; 1 cites it directly.
0 of 485 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K960413: Coherent Slimline Single Lumen Aspiration Needle Kit (1996), 483 descendants of its own
- K980685: Modified Versapulse Select HO:Yag and HO:Yag/ND:Yag Lasers (1998), 351 descendants of its own
- K990947: Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO: Yag/ND: Yag Surgical Lasers and  Delivery (1999), 350 descendants of its own
- K011703: Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength (HO:Yag/ND:Yag) Surgical Lasers and Delivery Devices (2001), 342 descendants of its own
- K050738: FT Fiber Optic Delivery Systems (2005), 225 descendants of its own

Source page: https://510kreport.com/device/K913136
Methodology: https://510kreport.com/methodology