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PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041348
510(k) Type
Traditional
Applicant
SMITHS MEDICAL
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/13/2004
Days to Decision
54 days
Submission Type
Summary

PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041348
510(k) Type
Traditional
Applicant
SMITHS MEDICAL
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/13/2004
Days to Decision
54 days
Submission Type
Summary