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CDI(R) 2000 BLOOD GAS MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884228
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1989
Days to Decision
115 days

CDI(R) 2000 BLOOD GAS MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884228
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1989
Days to Decision
115 days