# K945381: Nasopharyngoscopes, Bronchoscopes, Tracheoscp[ES and Esophagoscopes, Laryngoscopes, Oto-Telescopes

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Jan 18, 1995 after 77 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K030857: Mahe Pediatric Naso Pharyngoscope Its Associated and Ancillary Equipment and Endoscopic Accessories (2003), 1 descendant of its own
- K171402: KARL STORZ Slim Nasopharyngolaryngoscope (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K945381
Methodology: https://510kreport.com/methodology