# K023735: Lapman Laparoscope Manipulator System and Accessories, Model 900-001

- Pathway: 510(k) (Abbreviated)
- Applicant: Medsys, S.A.
- Decided: Aug 7, 2003 after 273 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931783 (1993). 4 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972699: Aesop 3000 System and Accessories, Computer Motion, Inc. (1997) Summary page 1.

## Most influential descendants
- K043284: Endoassist (2005), 2 descendants of its own
- K090340: Freehand (2009), 1 descendant of its own
- K102179: Enview (TM) (2010), 0 descendants of its own

## Indications for use
The LapMan Laparoscope Manipulator System and Accessories is indicated for use in General Surgery, Gynecology, and Urology where a laparoscope/endoscope is incorporated into the surgical procedure. The LapMan is indicated for specific laparoscopic surgical procedures as defined in the Operations Manual and should not be used for any other surgical procedure or purpose. The LapMan should only be used by qualified medical personnel, such as trained surgeons, gynecologists, urologists, and similarly-trained medical personnel trained in the use of laparoscopic/endoscopic devices.

Source page: https://510kreport.com/device/K023735
Methodology: https://510kreport.com/methodology