Company ยท US
Reprocessing Products Corp
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2013. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 20, 2013 | K123805 | E-Z CHEK BLOOD LEAK TEST STRIPS Reprocessing Products Corp | FJD |
| Jan 7, 2011 | 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 Reprocessing Products Corp | MNV |
| May 8, 2009 | K090338 | ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE Reprocessing Products Corp | MSY |
| Feb 10, 1999 | K974426 | POTENCY TEST STRIPS, INDICATOR TEST STRIPS Reprocessing Products Corp | LIF |
| Dec 7, 1998 | K974064 | MICRO X RESIDUAL TEST STRIPS Reprocessing Products Corp | MSY |
| Nov 30, 1995 | K950602 | PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS Reprocessing Products Corp | FJI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||