# K153542: Pelican Sling Retractor

- Pathway: 510(k) (Traditional)
- Applicant: Beacon Surgical, Inc.
- Decided: Sep 7, 2016 after 271 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: 2 generations back to K914190 (1992). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082291: A-Lap Set (a-Lap, Ezaxess, Trocar), Ezsurgical (2009) Summary page 5.
- (no number) Covidien: Auto suture Endo paddle retractor (Auto suture): named in the summary without a submission number

## Indications for use
The Pelican Sling Retractors have applications in a variety of gynecologic, general, urologic, thoracic, colorectal, laparoscopic and endoscopic procedures for the temporary retracting of internal structures such as organs or tissue.

Source page: https://510kreport.com/device/K153542
Methodology: https://510kreport.com/methodology