FDA Approvals - Signalife Submits Fidelity 200 Cardiac Event Recorder Pre-Market Notification to
Signalife Submits Fidelity 200 Cardiac Event Recorder Pre-Market Notification to FDA (PR Newswire via Yahoo! Finance)
Signalife, Inc. has announced that it has submitted its Fidelity 200 Cardiac Event Recorder 510K pre-market notification to the FDA.
Barr receives two approvals for Enjuvia (Pharmaceutical Business Review)
Barr Pharmaceuticals subsidiary Duramed Pharmaceuticals has received two additional approvals from the FDA for its menopause product Enjuvia.