MINNEAPOLIS--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer of specialty infusion devices, announced today that its CADD-Solis v3.0 PIB Ambulatory Infusion Pump has ...
ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to launch ...
ROCHESTER HILLS, Mich.--(BUSINESS WIRE)--InfuSystem Holdings, Inc. (NYSE American: INFU) (“InfuSystem” or the “Company”), a leading national health care service provider, facilitating outpatient care ...
Smiths Medical has issued a Class I recall for certain CADD-Solis and CADD-Solis VIP ambulatory infusion pumps due to multiple issues that could interrupt or delay medication delivery. The FDA ...
Smiths Medical has recalled ambulatory infusion pumps to provide updated use instructions to providers after identifying issues with potential false alarms as well as two other problems that could ...
The FDA gave 510(k) clearance to Smiths Medical's "smart" infusion pump, which includes error-prevention software for a number of therapies. The company says its CADD-Solis VIP pump improves on the ...
FDA Clears Smiths Medical to Market Patient-Controlled Pain Pump The U.S. Food and Drug Administration has given St. Paul, Minn.-based Smiths Medical 510 (k) clearance to market its CADD-Solis Pain ...
Today, Smiths Medical’s correction of the CADD-Solis Li-ion rechargeable battery packs was deemed FDA Class I. The CADD-Solis Li-ion rechargeable battery packs are lithium-ion battery packs used as an ...
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