# K002214: Sinuscope and Baccessories

- Pathway: 510(k) (Traditional)
- Applicant: Pollux Endoscopy, Inc.
- Decided: Nov 21, 2000 after 120 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.
8 later devices descend from it; 2 cite it directly.
0 of 9 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
- K100577: Acclarent Cyclops Multi-Angle Endoscope (2011), 4 descendants of its own
- K110097: Acclarent Cyclops Multi-Angle Endoscope (2011), 3 descendants of its own
- K063078: Microendoscope (2006), 2 descendants of its own
- K132433: Acclarent Cyclops Multi-Angle Endoscope (2014), 1 descendant of its own
- K100533: Vista Endoscope,89 CM, 56CM , Scout Blunt-Tipped Guide- 106 CM, 86 CM, 53 CM, Models FG0027, FG0031, FG0029, FG 0028, (2011), 1 descendant of its own

Source page: https://510kreport.com/device/K002214
Methodology: https://510kreport.com/methodology