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PORTEX PERCUTANEOUS TRACHEOSTOMY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060945
510(k) Type
Traditional
Applicant
Smiths Medical International
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/19/2006
Days to Decision
74 days
Submission Type
Statement

PORTEX PERCUTANEOUS TRACHEOSTOMY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060945
510(k) Type
Traditional
Applicant
Smiths Medical International
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/19/2006
Days to Decision
74 days
Submission Type
Statement