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HSMN NewsFeed - 10 Jun 2021
Nuvo Group Receives 510(k) FDA Clearance for Remote Monitoring of Uterine Activity
Nuvo Group Receives 510(k) FDA Clearance for Remote Monitoring of Uterine Activity
HSMN NewsFeed - 1 Jun 2017
GenePOC Announces FDA Clearance for Revogene(TM) Instrument and its GBS LB Test
GenePOC Announces FDA Clearance for Revogene(TM) Instrument and its GBS LB Test
HSMN NewsFeed - 7 Jan 2015
Philips receives FDA 510(k) clearance for its latest Avalon CL Fetal Monitoring solution
Philips receives FDA 510(k) clearance for its latest Avalon CL Fetal Monitoring solution
HSMN NewsFeed - 30 Dec 2013
Quidel Receives FDA Clearance for Its Hand-Held Molecular Diagnostic Test - AmpliVue(R) Group B Strep Assay
Quidel Receives FDA Clearance for Its Hand-Held Molecular Diagnostic Test - AmpliVue(R) Group B Strep Assay
HSMN NewsFeed - 2 Apr 2007
FDA Approves Rhophylac(R) for the Treatment of Immune Thrombocytopenic Purpura (ITP)
FDA Approves Rhophylac(R) for the Treatment of Immune Thrombocytopenic Purpura (ITP)
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