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PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA

Page Type
Cleared 510(K)
510(k) Number
K030381
510(k) Type
Traditional
Applicant
PORTEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/27/2003
Days to Decision
203 days
Submission Type
Summary

PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA

Page Type
Cleared 510(K)
510(k) Number
K030381
510(k) Type
Traditional
Applicant
PORTEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/27/2003
Days to Decision
203 days
Submission Type
Summary