# K992437: Schoelly Rigid Endoscopes

- Pathway: 510(k) (Traditional)
- Applicant: Fiber Imaging Technologies, Inc.
- Decided: Sep 14, 1999 after 54 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.
21 later devices descend from it; 2 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K060899: Flexilux II Cystoscope and Hysteroscope (2007), 19 descendants of its own
- K150158: Schoelly Cystoscopes/Hysteroscopes and Accessories (2015), 18 descendants of its own
- K161110: ClearPetra Suction-Evacuation Sheath (2016), 7 descendants of its own
- K170660: Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula (2017), 5 descendants of its own
- K183020: Endosee System (2019), 4 descendants of its own

## Indications for use
The Schoelly Laparoscope is indicated for examinat:ion of body cavities, holow organs, and canals, and using additional accessories, to perform various diagnostic and therapeutic procedures,

Source page: https://510kreport.com/device/K992437
Methodology: https://510kreport.com/methodology