Last synced on 25 January 2026 at 3:41 am

COBE PATIENT MONITORING PRODUCTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921343
510(k) Type
Traditional
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1993
Days to Decision
292 days
Submission Type
Summary

COBE PATIENT MONITORING PRODUCTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921343
510(k) Type
Traditional
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1993
Days to Decision
292 days
Submission Type
Summary