Last synced on 14 November 2025 at 11:06 pm

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