Rockwell Medical Technologies, Inc.
Rockwell Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2006.
Top product codes for Rockwell Medical Technologies, Inc.
Recent clearances by Rockwell Medical Technologies, Inc.
- K062399 — ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE
- K023985 — ACIDIFIED COMPONENT CONCENTRATES FOR BICARBONATE DIALYSIS CONTAINING DI-ACETATE
- K022521 — BICARBONATE DIALYSATE CONCENTRATE MIXER, MODEL 50 GALLON & 100 GALLON
- K022500 — DRI-SATE DRY ACID CONCENTRATE FOR BICARBONATE DIALYSATE
- K983618 — DRI-SATE MIXER FOR PREPARATION OF ACIDIFIED DIALYSATE CONCENTRATE
Data sourced from openFDA. This site is unofficial and independent of the FDA.