# K062968: Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series

- Pathway: 510(k) (Special)
- Applicant: Medsys, S.A.
- Decided: Jan 3, 2007 after 96 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.
4 later devices descend from it; 1 cites it directly.
0 of 9 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
- K131375: Autolap System (2013), 3 descendants of its own
- K152848: Autolap System (2015), 2 descendants of its own
- K242323: Maestro System (REF100) (2025), 1 descendant of its own
- K250984: Maestro System (REF100) (2025), 0 descendants of its own

## Indications for use
The LapMan can be used during the laparoscopic procedures listed below and should not be used for any other surgical procedure or purpose. 1. General surgery: laparoscopic cholecystectomy, laparoscopic Nissen Fundoplication, laparoscopic inguinal hernia repair, laparoscopic gastric banding. 2. Gynaecology: laparoscopic adnexal surgery (ovarian cystectomy, oophorectomy, adnexectomy, salpingectomy, salpingoneostomy, tubal reanastomosis), laparoscopic management of ectopic pregnancy, laparoscopic treatment of endometriosis, laparoscopic myomectomy, laparoscopic hysterectomy, laparoscopic colposuspension 3. Urology: laparoscopic prostatectomy.

Source page: https://510kreport.com/device/K062968
Methodology: https://510kreport.com/methodology