# K143221: Schoelly Laparoscope

- Pathway: 510(k) (Special)
- Applicant: Schoelly Fiberoptic GmbH
- Decided: Dec 5, 2014 after 25 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: 1 generation back to K992437 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992437: Schoelly Rigid Endoscopes, Fiber Imaging Technologies, Inc. (1999) Summary page 4.

## Indications for use
The Schoelly Laparoscope is indicated for examination of body cavities, hollow organs, and canals, and using additional accessories, to perform various diagnostic and therapeutic procedures.

Source page: https://510kreport.com/device/K143221
Methodology: https://510kreport.com/methodology