# K113062: Endoservice Endoscopic Instruments & Accessories and Minimally Invasive GI and GU Devices

- Pathway: 510(k) (Traditional)
- Applicant: Endoservice Optical Instruments GmbH
- Decided: Aug 21, 2012 after 312 days
- Product code: FBP (Telescope, Rigid, Endoscopic)
- 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 K012660 (2001). 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)
- K012660: Gimmi'alpha' Endoscopes & Accessories, Gimmi GmbH (2001) Summary page 1.

## Indications for use
Endoservice Endoscopic Instruments & Accessories and Minimally Invasive GI and GU Devices are intended to be used by qualified physicians to provide access and visualization of internal structures such as bladder, urethra, kidneys, prostate and for manipulating soft tissue (grasping, cutting, coagulating, dissecting, and suturing).

Source page: https://510kreport.com/device/K113062
Methodology: https://510kreport.com/methodology