# K093194: MGB Disposable Retrieval Bag Lapbag

- Pathway: 510(k) (Traditional)
- Applicant: Mgb Endoskopische Gerate GmbH (Berlin)
- Decided: Mar 3, 2010 after 145 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K171726: LapBag (2017), 0 descendants of its own

## Indications for use
The MGB LAPBAG sterile retrieval bag for Endoscopic surgery is intended to be used for: General surgery Abdominal surgery Gynecological surgery Thoracic minimally invasive procedures. The Specimen Retrieval Bag is indicated for use in endloscopic procedures to allow tissues or debris to be removed from the abdominal cavity.

Source page: https://510kreport.com/device/K093194
Methodology: https://510kreport.com/methodology