Biosense Webster Announces FDA Submission for Approval of the Varipulse Platform
All 20 participants in a 12-month follow-up study attained acute success from ablation procedures.
Source: pharmacytimes.com
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Biosense Webster submits Varipulse PFA system for FDA approval
Johnson & Johnson MedTech's Biosense Webster announced today that it submitted its Varipulse platform to the FDA for premarket approval.
Source: massdevice.com
Biosense Webster Announces CE Mark approval in Europe for VARIPULSE™ Pulsed Field Ablation (PFA) Platform
/PRNewswire/ -- Biosense Webster, Inc., a global leader in cardiac arrhythmia treatment and part of Johnson & Johnson MedTech, today announced European CE mark...
Source: prnewswire.com
Börse Express - Biosense Webster Announces CE Mark approval in Europe for VARIPULSE™ Pulsed Field Ablation (PFA) Platform
Biosense Webster, Inc., a global leader in cardiac arrhythmia treatment and part of Johnson & Johnson MedTech, today announced European CE mark approval of the VARIPULSE™ Platform for the treatment of symptomatic drug refractory recurrent paroxysmal atrial fibrillation (AF) using pulsed field ablation (PFA). The VARIPULSE™ Platform is comprised...
Source: boerse-express.com
J&J's Biosense Webster's Varipulse PFA system wins CE mark
J&J MedTech's Biosense Webster unit announced today that it won CE mark approval for its Varipulse pulsed field ablation platform.
Source: massdevice.com