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ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING

Page Type
Cleared 510(K)
510(k) Number
K895763
510(k) Type
Traditional
Applicant
HEALTHDYNE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1989
Days to Decision
87 days

ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING

Page Type
Cleared 510(K)
510(k) Number
K895763
510(k) Type
Traditional
Applicant
HEALTHDYNE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1989
Days to Decision
87 days