# Meditec Co., Ltd.

- Location (FDA's records): Sunnamcity, Kyunggido, KR
- FDA decisions: 8 (1983–2004): 8 510(k) clearances
- Names in FDA's records: Meditec Co., Ltd. (4); Meditec, Inc. (4)
- Product codes: DXN (4), GEX (2), HQF (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Sein Electronics Co., Ltd.: 1 (https://510kreport.com/company/sein-electronics)
- Omron Healthcare, Inc.: 1 (https://510kreport.com/company/omron-healthcare)

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

## Its most-cited devices
- K992328: Fuzzy Automatic Blood Pressure Monitor Models MD-750, MD-770, MD-800 (1999), cited by 2

## Recent decisions
- K041789: Noninvasive Blood Pressure Monitor, Models MD-880B and MD-900T (Jul 15, 2004)
- K002655: Digital Blood Pressure Monitor, Model MD-550 (Sep 6, 2000)
- K992328: Fuzzy Automatic Blood Pressure Monitor Models MD-750, MD-770, MD-800 (Jul 21, 1999)
- K990380: (1) Digital Blood Pressure Monitor, Model MD-250; (2) Fully Automatic Blood Pressure Monitor, Model MD-700 (Feb 22, 1999)
- K854833: MDS-83 in Dermatological/Plastic Surgery Applicati (Apr 4, 1986)
- K852234: MDS 83 Ophthalmic Dye Laser System (Aug 1, 1985)
- K832983: Dermolas (Apr 23, 1984)
- K837030: Model ML-4000 Ophthalmic Laser with Fiber Optic Delivery System (Jan 24, 1983)

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