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COBE PATIENT MONITORING PRODUCTS

Page Type
Cleared 510(K)
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)
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