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TERUMO SURFLASH SAFETY I.V. CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122544
510(k) Type
Traditional
Applicant
TERUMO Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/5/2012
Days to Decision
15 days
Submission Type
Summary

TERUMO SURFLASH SAFETY I.V. CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122544
510(k) Type
Traditional
Applicant
TERUMO Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/5/2012
Days to Decision
15 days
Submission Type
Summary