Vanguard Biomedical Corp.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960733 | MINISTICK PREGNANCY TEST | LCX | 1996-05-01 | View |
| 510(k) | K960233 | MINICLINIC OVULATION PREDICTOR | CEP | 1996-04-23 | View |
| 510(k) | K930014 | PROCLINIC ONE-STEP DIPSTICK PREGNANCY TEST | JHI | 1993-03-25 | View |
| 510(k) | K914254 | HOMECLINIC ONE STEP PREGNANCY TEST | LCX | 1991-10-17 | View |
| 510(k) | K914253 | PROCLINIC ONE STEP PREGNANCY TEST | JHI | 1991-10-11 | View |
| 510(k) | K910351 | MINICLINIC OVULATION PREDICTION TEST | CEP | 1991-03-21 | View |
| 510(k) | K895560 | MODIFIED HOMECLINIC PREGNANCY TEST | LCX | 1989-11-13 | View |
| 510(k) | K894012 | MINICLINIC PREGNANCY TEST | JHI | 1989-07-25 | View |
| 510(k) | K891762 | MINICLINIC OVULATION PREDICTION TEST | CEP | 1989-07-20 | View |
| 510(k) | K883826 | HOME CLINIC PREGNANCY TEST | LCX | 1988-11-29 | View |
No matching devices.
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