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NEWPORT WAVE VENTILATOR MODEL E200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901785
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1990
Days to Decision
114 days

NEWPORT WAVE VENTILATOR MODEL E200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901785
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1990
Days to Decision
114 days