FDA 510(k) Applications Submitted by Di-Chem, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171015 | 04/04/2017 | Citryte | Di-Chem, Inc. |
| K202508 | 08/31/2020 | Hemo-Lyte C Cartridge | Di-Chem, Inc. |
| K012328 | 07/23/2001 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE POWDER | DI-CHEM, INC. |
| K012547 | 08/07/2001 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION | DI-CHEM, INC. |
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