# K133393: Gelpoint Path Transanal Access Platform

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources Corp.
- Decided: Jan 2, 2014 after 58 days
- Product code: FER (Anoscope And Accessories)
- 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: 8 generations back to K940232 (1994). 30 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070915: Sapimed Disposable Sigmoidoscope, Sapimed S.P.A. (2007) Summary page 1.
- K110792: Gelpoint Path, Applied Medical Resources Corp. (2011) Summary page 1.

## Most influential descendants
- K171701: GelPOINT Path Transanal Access Platform (2017), 0 descendants of its own

## Indications for use
The GeIPOINT Path Transanal Access Platform is indicated for multiple instrument or camera access through the anus to perform various diagnostic and therapeutic procedures by using additional accessories.

Source page: https://510kreport.com/device/K133393
Methodology: https://510kreport.com/methodology