Response Biomedical Corp.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K093116 | MODIFICATION TO: RAMP INFLUENZA A/B ASSAY | PSZ | 2009-10-21 | View |
| 510(k) | K091235 | RAMP RSV ASSAY | GQG | 2009-07-24 | View |
| 510(k) | K063662 | RAMP NT-PROBNP ASSAY | NBC | 2008-07-21 | View |
| 510(k) | K071591 | RAMP INFLUENZA A/B ASSAY | PSZ | 2008-04-16 | View |
| 510(k) | K033747 | RAMP CK-MB ASSAY | JHX | 2004-05-17 | View |
| 510(k) | K033745 | RAMP TROPONIN I ASSAY | MMI | 2004-05-17 | View |
| 510(k) | K012040 | RAMP MYOGLOBIN ASSAY | DDR | 2001-12-18 | View |
No matching devices.
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