# K073452: Modification to: Aragon Surgical Lapcap

- Pathway: 510(k) (Special)
- Applicant: Aragon Surgical, Inc.
- Decided: Jan 11, 2008 after 32 days
- Product code: HIF (Insufflator, Laparoscopic)
- Device class: 2
- Regulation: 21 CFR 884.1730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K852726 (1985). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070651: Aragon Surgical Lapcap, Aragon Surgical, Inc. (2007) Summary page 1.

## Most influential descendants
- K212786: LevaLap Laparoscopic Access Device (2022), 0 descendants of its own

## Indications for use
The Aragon Surgical LapCap is intended for use in the pen-umbilical region of the abdominal wall with a Veress needle for the establishment of a pneumoperitoneum during gynecologic (pelvic) and general surgical (intraabdominal) laparoscopic procedures.

Source page: https://510kreport.com/device/K073452
Methodology: https://510kreport.com/methodology