DEKA Research & Development

DEKA Research & Development holds 3 FDA 510(k) medical device clearances, first cleared 2016, most recent 2020.

Top product codes for DEKA Research & Development

Recent clearances by DEKA Research & Development

K191313 — Unity Subcutaneous Infusion System for RemodulinCode QJY·2020-02-21
K190182 — Unity Subcutaneous Delivery System for RemodulinCode FRN·2019-05-06
K153760 — Volumetric Infusion ControllerCode LDR·2016-10-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.