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FAST1™ Intraosseous Infusion System; FASTResponder™ Sternal Intraosseous Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180588
510(k) Type
Traditional
Applicant
Teleflex Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
42 days
Submission Type
Summary

FAST1™ Intraosseous Infusion System; FASTResponder™ Sternal Intraosseous Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180588
510(k) Type
Traditional
Applicant
Teleflex Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
42 days
Submission Type
Summary