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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)
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)
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