Company ยท US
Di-Chem, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 2022. 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 |
|---|---|---|---|
| Aug 12, 2022 | K202508 | Hemo-Lyte C Cartridge Di-Chem, Inc. | KPO |
| Oct 13, 2017 | K171015 | Citryte Di-Chem, Inc. | KPO |
| Jan 18, 2002 | K012547 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION Di-Chem, Inc. | KPO |
| Jan 18, 2002 | K012328 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE POWDER Di-Chem, Inc. | KPO |
| Apr 9, 1991 | K905217 | FORMASURE TEST REAGENT Di-Chem, Inc. | LIF |
| Nov 17, 1982 | K823103 | DIALYSATE ADDITIVES-POWDER/LIQUID Di-Chem, Inc. | KPO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||