Reprocessing Products Corp
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K123805 | E-Z CHEK BLOOD LEAK TEST STRIPS | FJD | 2013-03-20 | View |
| 510(k) | K101750 | RPC E-Z CHEK 6.8-8.5 PH TEST STRIPS, MODEL K100-0117 AND E-Z CHEK 0-14 PH TEST STRIPS, MODEL K100-0104 | MNV | 2011-01-07 | View |
| 510(k) | K090338 | ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE | MSY | 2009-05-08 | View |
| 510(k) | K974426 | POTENCY TEST STRIPS, INDICATOR TEST STRIPS | LIF | 1999-02-10 | View |
| 510(k) | K974064 | MICRO X RESIDUAL TEST STRIPS | MSY | 1998-12-07 | View |
| 510(k) | K950602 | PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS | FJI | 1995-11-30 | View |
No matching devices.
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