# Ameditech, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 14 (2001–2011): 14 510(k) clearances
- Product codes: DKZ (5), DJG (2), DIO (2), LAF (1), LCM (1), DIS (1), LCX (1), LDJ (1)
- Predicates its devices cite: 6 (6 its own); citations of its devices by later devices: 9 (6 its own)
- Recalls linked to its devices: 87 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Worldwide Medical Corp.: 2 (https://510kreport.com/company/worldwide-medical)
- First Check Diagnostics, LLC: 1 (https://510kreport.com/company/first-check-diagnostics)

## Its most-cited devices
- K040092: Ameditech Immu Test Drug Screen Panel (2004), cited by 2
- K050186: Ameditech Immutest Multi-Drug Screen Panel Iii (2005), cited by 2
- K042975: Ameditech Immutest Multi-Drug Screen Panel II (2004), cited by 2
- K053175: Ameditech Drugsmartcup (2005), cited by 1
- K113046: Ameditech Immutest Milti-Drug Screen (2011), cited by 1
- K063015: Ameditech Immutest Multi-Drug Screen Bup/PPX/COC150 (2006), cited by 1

## Recent decisions
- K113501: Ameditech Checkcup Multi Drug Test (Flat/Round Cup) (Dec 5, 2011)
- K113046: Ameditech Immutest Milti-Drug Screen (Nov 10, 2011)
- K063015: Ameditech Immutest Multi-Drug Screen Bup/PPX/COC150 (Dec 20, 2006)
- K053175: Ameditech Drugsmartcup (Dec 8, 2005)
- K050186: Ameditech Immutest Multi-Drug Screen Panel Iii (Mar 4, 2005)
- K042975: Ameditech Immutest Multi-Drug Screen Panel II (Dec 29, 2004)
- K040092: Ameditech Immu Test Drug Screen Panel (Mar 8, 2004)
- K023126: Ameditech Immutest HCG Pregancy Test (Nov 18, 2002)

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