# K874215: Endoscopes for Sinus Surgery

- Pathway: 510(k) (Traditional)
- Applicant: Richards Medical Co., Inc.
- Decided: Jan 4, 1988 after 80 days
- Product code: EOB (Nasopharyngoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K981751: Sinuscope and Accessories (1998), 3 descendants of its own
- K032822: Asap Sinuscope 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0 (2004), 2 descendants of its own
- K082667: Visionsense Stereoscopic Vision System (VS System) (2008), 1 descendant of its own
- K162410: TIPCAM 1S 3D System (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K874215
Methodology: https://510kreport.com/methodology