# K951196: FNL-10P, Fiber Nasoparhyngoscope

- Pathway: 510(k) (Traditional)
- Applicant: Pentax Precision Instrument Corp.
- Decided: Apr 7, 1995 after 22 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
- K992526: Flexible Nasopharyngo-Laryngoscopes, Flexible Bronchoscope (1999), 3 descendants of its own
- K132039: Ergo-Flex Laryngo-Nasopharyngoscope EF-N and EF-N Slim (2014), 1 descendant of its own
- K150248: ORL Video NasoPharyngo-Larngoscope (2015), 0 descendants of its own
- K070580: Nasopharyngoscope, Bronchoscope (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K951196
Methodology: https://510kreport.com/methodology