Last synced on 21 June 2024 at 11:04 pm

NEWPORT E500 WAVE VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030780
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2004
Days to Decision
318 days
Submission Type
Summary

NEWPORT E500 WAVE VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030780
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2004
Days to Decision
318 days
Submission Type
Summary