Last synced on 14 November 2025 at 11:06 pm

Shiley™ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440, 87445, 87450, 87455, 87460, 87465, 87470, 87475, 87480, 87485, 87490, 87495, 87410)

Page Type
Cleared 510(K)
510(k) Number
K233341
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2024
Days to Decision
234 days
Submission Type
Summary

Shiley™ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440, 87445, 87450, 87455, 87460, 87465, 87470, 87475, 87480, 87485, 87490, 87495, 87410)

Page Type
Cleared 510(K)
510(k) Number
K233341
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2024
Days to Decision
234 days
Submission Type
Summary