Bio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism

Press/Media: Press / Media

PeriodAug 24 2016

Media coverage

11

Media coverage

  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletPR Newswire
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletPR Newswire
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletPR Newswire
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletWorldNetDaily
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletBioSpace
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletYahoo! Finance
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletYahoo! Singapore
    CountrySingapore
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletTickerTech.com
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletDaily Times Leader
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outletStock Nod
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers
  • TitleBio2 Medical® Announces 510(k) Clearance from the FDA for the Angel® Catheter, the First Ever Prophylactic Use Indication for a Medical Device for Pulmonary Embolism
    Media name/outlet9&10 News
    CountryUnited States
    Date8/24/16
    PersonsJohn G Myers