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VENTURI VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982174
510(k) Type
Traditional
Applicant
CARDIOPULMONARY CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
6/24/1998
Days to Decision
7 days

VENTURI VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982174
510(k) Type
Traditional
Applicant
CARDIOPULMONARY CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
6/24/1998
Days to Decision
7 days