# K915804: Propper Laryngoscope Blades W Fiber Optic Illum.

- Pathway: 510(k) (Traditional)
- Applicant: Propper Mfg. Co., Inc.
- Decided: Mar 20, 1992 after 87 days
- Product code: CCW (Laryngoscope, Rigid)
- Device class: 1
- Regulation: 21 CFR 868.5540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K163412: Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL) (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K915804
Methodology: https://510kreport.com/methodology