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CARDIOCAP II TM CH-RESP MONITORS

Page Type
Cleared 510(K)
510(k) Number
K904355
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/23/1991
Days to Decision
241 days

CARDIOCAP II TM CH-RESP MONITORS

Page Type
Cleared 510(K)
510(k) Number
K904355
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/23/1991
Days to Decision
241 days