# K864821: Airway Fiberscopes, Models LS-9, 0L-1, 0L-2 & PL-2

- Pathway: 510(k) (Traditional)
- Applicant: Reichert-Jung, Inc.
- Decided: Feb 10, 1987 after 63 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.
16 later devices descend from it; 1 cites it directly.
0 of 17 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
- K080622: Entity Nasoview Led Nasopharyngoscope, Model 006105 (2008), 15 descendants of its own
- K091829: PLS Portable Light Source (2009), 9 descendants of its own
- K130503: Pathassist Led Light Fiber (2013), 6 descendants of its own
- K141916: Pathassist Led Light Fiber (2014), 5 descendants of its own
- K100577: Acclarent Cyclops Multi-Angle Endoscope (2011), 4 descendants of its own

Source page: https://510kreport.com/device/K864821
Methodology: https://510kreport.com/methodology