# Accu-Line

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1983–1983): 4 510(k) clearances
- Product codes: KNT (1), KRA (1), FZZ (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K831847: Jejunostomy Kit (Aug 31, 1983)
- K831636: Percutaneous Introducer Kit (Aug 24, 1983)
- K831637: Accu-Flush (Jun 30, 1983)
- K830298: Accu-Line Surgical Marker (Jun 2, 1983)

Source page: https://510kreport.com/company/accu-line