Last synced on 4 February 2023 at 10:33 pm

ADVENT VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884793
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1989
Days to Decision
208 days

ADVENT VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884793
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1989
Days to Decision
208 days