# K061387: Veresure Bell

- Pathway: 510(k) (Traditional)
- Applicant: Veresure, Inc.
- Decided: Jul 21, 2006 after 64 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: 1 generation back to K852726 (1985). 3 ancestors in all.
5 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)
- K003703: Taut-Insufflation Needle, Taut, Inc. (2001) Summary page 1.
- K983925: Endopath Ultra Veress Needle, Ethicon Endo-Surgery, Inc. (1999) Summary page 1.
- K852726: Allis Tissue Forceps, 4X5 Teeth, 6+SS 410 or 420, The Huxley Instrument Corp. (1985) Summary page 1.

## Most influential descendants
- K070651: Aragon Surgical Lapcap (2007), 4 descendants of its own
- K233020: TauTona Pneumoperitoneum Assist Device (TPAD) (2024), 1 descendant of its own
- K073452: Modification to: Aragon Surgical Lapcap (2008), 1 descendant of its own
- K242536: TauTona Pneumoperitoneum Assist Device (TPAD) (2024), 0 descendants of its own
- K212786: LevaLap Laparoscopic Access Device (2022), 0 descendants of its own

## Indications for use
The VereSure Bell is intended for use in the penj-umbilical region of the abdominal wall with a Veress needle for the establishment of pneumoperitoneum during gynecologic laparoscopic procedures.

Source page: https://510kreport.com/device/K061387
Methodology: https://510kreport.com/methodology