# K020702: O'regan Disposable Anoscope

- Pathway: 510(k) (Traditional)
- Applicant: Canadian Theatre Products, Ltd.
- Decided: Mar 29, 2002 after 25 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: 1 generation back to K993738 (2000). 1 ancestor in all.
13 later devices descend from it; 2 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993738: Dispos-a-Scope, Dispos-A-Scope (2000) Summary page 1.

## Most influential descendants
- K070913: Self-Light Disposable Anoscope (2007), 11 descendants of its own
- K080132: THD Disposable Anoscope/Proctoscope (2008), 6 descendants of its own
- K091490: Family of THD Disposable Anoscopes/Proctoscopes/Rectoscopes (2009), 4 descendants of its own
- K103647: THD Disposable Anoscopes, Proctoscopes and Rectoscopes (2011), 3 descendants of its own
- K121135: THD Anoscope, Proctoscope, Rectoscope, Rectoscope and Light-Scope (2012), 1 descendant of its own

## Indications for use
The O’Regan Disposable Anoscope is intended for physician use to examine the anal sphincter and anus, and, using additional accessories, to perform various diagnostic and therapeutic procedures.

Source page: https://510kreport.com/device/K020702
Methodology: https://510kreport.com/methodology