# K883414: Laryngoscope Blades

- Pathway: 510(k) (Traditional)
- Applicant: Truphatek, Ltd.
- Decided: Aug 19, 1988 after 4 days
- Product code: CCW (Laryngoscope, Rigid)
- Device class: 1
- Regulation: 21 CFR 868.5540
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K984101: Flexiblade (1999), 0 descendants of its own

## Recalls of this device
- Jun 15, 2006 · Not classified · Z-1225-06: Teleflex Medical has identified that the product may malfunction, causing the handle to heat up. There is a potential for the heated handle to burn the user.

Source page: https://510kreport.com/device/K883414
Methodology: https://510kreport.com/methodology