Meditec Co., Ltd.
Sunnamcity, Kyunggido, KR
Meditec Co., Ltd. appears in FDA device records in Sunnamcity, Kyunggido, KR. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Meditec Co., Ltd. between 1983 and 2004. The busiest year on record is 1999, with 2. The most recent is 2004, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| 1999 | 2 |
| 2000 | 1 |
| 2004 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K041789 | NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T | DXN | Substantially Equivalent | |
| K002655 | DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-550 | DXN | Substantially Equivalent | |
| K992328 | FUZZY AUTOMATIC BLOOD PRESSURE MONITOR MODELS MD-750, MD-770, MD-800 | DXN | Substantially Equivalent | |
| K990380 | (1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250; (2) FULLY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL MD-700 | DXN | Substantially Equivalent | |
| K854833 | MDS-83 IN DERMATOLOGICAL/PLASTIC SURGERY APPLICATI | GEX | Substantially Equivalent | |
| K852234 | MDS 83 OPHTHALMIC DYE LASER SYSTEM | HQF | Substantially Equivalent | |
| K832983 | DERMOLAS | GEX | Substantially Equivalent | |
| K837030 | MODEL ML-4000 OPHTHALMIC LASER WITH FIBER OPTIC DELIVERY SYSTEM | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain