Mizuho USA, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Advertisement
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K060825 | MULTI-USE ELECTRONIC PREGNANCY TEST | LCX | 2006-06-19 | View |
| 510(k) | K043231 | PROOF POSITIVE ELECTRONIC PREGNANCY TEST | LCX | 2005-04-25 | View |
| 510(k) | K000844 | ABSOLUTE HCG PREGNANCY TEST | DHA | 2000-06-16 | View |
| 510(k) | K964002 | NATURALE HCG PREGNANCY TES | LCX | 1996-11-07 | View |
| 510(k) | K943859 | QUICK CHECKER HCG PREGNANCY TEST | JHI | 1995-02-10 | View |
| 510(k) | K945568 | HCG MIDSTREAM PREGNANCY TEST | LCX | 1995-01-17 | View |
| 510(k) | K931997 | HCG MIDSTREAM PREGNANCY TEST | LCX | 1993-09-10 | View |
No matching devices.
Advertisement