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BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K030570
510(k) Type
Traditional
Applicant
Portex , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
205 days
Submission Type
Summary

BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K030570
510(k) Type
Traditional
Applicant
Portex , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
205 days
Submission Type
Summary