# LZB: Finger Cot

- Device class: 1; regulation: 21 CFR 880.6250; FDA's rule: 510(k) exempt
- FDA decisions: 5
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1990: 1
- 1991: 1
- 1998: 1
- 2000: 1
- 2005: 1

## Most-cited predicates
- K992539: Percuguard (2000), cited by 2
- K980827: Latex Finger Cot, Powder-Free, with Protein Labeling (1998), cited by 1

Source page: https://510kreport.com/product-code/LZB
Data by year (CSV): https://510kreport.com/product-code/LZB.csv