# Diag Corp.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 9 (1980–1999): 9 510(k) clearances
- Product codes: DTB (5), DYB (2), DSA (1), LDF (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Daig Corp.: 1 (https://510kreport.com/company/daig)

## Firms that cite its devices most
- Vanguard Medical Concepts, Inc.: 1 (https://510kreport.com/company/vanguard-medical-concepts)

## Its most-cited devices
- K910645: Disposable Patient Cable (1991), cited by 1

## Recent decisions
- K984062: Seal-Away Hemostasis Adapter, Model 406229 (Mar 24, 1999)
- K911883: Daig Fast Cath (TM) Transseptal Sheath Introducer (Nov 29, 1991)
- K910645: Disposable Patient Cable (May 7, 1991)
- K852446: Endocardial Screw-in Lead with Platinum Porous Tip (Sep 17, 1985)
- K820003: Cardiovascular Temp. Pacemaker Elec (Mar 26, 1982)
- K820262: Permanent & Temporary Pacemaker Electr. (Mar 12, 1982)
- K812905: Permanent Endocard. Unipolar Tined Lead (Feb 4, 1982)
- K812270: Perm. Endocardial Unipolar Tined Atrial (Sep 16, 1981)

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