Last synced on 19 July 2024 at 11:05 pm

ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821456
510(k) Type
Traditional
Applicant
LIFE-LINE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1982
Days to Decision
34 days

ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821456
510(k) Type
Traditional
Applicant
LIFE-LINE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1982
Days to Decision
34 days