# Metronic, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (1983–2003): 4 510(k) clearances
- Product codes: DTD (1), IYX (1), DTB (1), BXB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K911827: Model 5866-9M & Model 6981M (1991), cited by 1

## Recent decisions
- K031210: Model 4951M Myocardial Unipolar Lead (May 16, 2003)
- K911827: Model 5866-9M & Model 6981M (Jul 23, 1991)
- K874884: Medtronic (R) Orthoflex (TM) (Jan 28, 1988)
- K832505: Image Processing Sys A3 (Sep 12, 1983)

Source page: https://510kreport.com/company/metronic