# K151990: Tissue Removal System

- Pathway: 510(k) (Traditional)
- Applicant: Boehringer Laboratories, LLC
- Decided: Sep 11, 2015 after 53 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: 3 generations back to K910914 (1991). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150781: Tissue Removal Pouch, Boehringer Laboratories, LLC (2015) Summary page 4.

## Indications for use
The Tissue Removal System is indicated for the contained removal of tissue, including contained manual tissue sectioning, during minimally invasive surgical procedures.

Source page: https://510kreport.com/device/K151990
Methodology: https://510kreport.com/methodology