Last synced on 1 July 2022 at 11:04 pm

BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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