Baxter gets 510(k) clearance for syringe pump, spurring optimism of faster FDA review process

Baxter gets 510(k) clearance for syringe pump, spurring optimism of faster FDA review process

Submitted by admin on September 1, 2022 - 10:41am
Source: 
Medtech Dive
News Tags: 
Baxter International
devices
Medtech
FDA
Novum IQ
infusion pumps
Headline: 
Baxter gets 510(k) clearance for syringe pump, spurring optimism of faster FDA review process
snippet: 

Baxter has received 510(k) clearance from the Food and Drug Administration for its Novum IQ syringe infusion pump (SYR) with Dose IQ Safety Software, opening up a new market that J.P. Morgan analysts value at as much as $200 million.

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