# Dip, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 3 (1981–1981): 3 510(k) clearances
- Product codes: DYB (2), KPE (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Inrad: 1 (https://510kreport.com/company/inrad)

## Its most-cited devices
- K812852: Set for Aseptic Decanting of a Flex I.V (1981), cited by 1

## Recent decisions
- K813019: Percutaneous Introducer: Seldinger Style (Nov 16, 1981)
- K812973: Percutaneous Introducer Cournand Style (Nov 16, 1981)
- K812852: Set for Aseptic Decanting of a Flex I.V (Nov 2, 1981)

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