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TRANSDUCER FOR ULTRASOUND FETAL MONITORING, MODELS FM10833 AND FM10834

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040819
510(k) Type
Traditional
Applicant
AMERICAN I.V. PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2004
Days to Decision
139 days
Submission Type
Summary

TRANSDUCER FOR ULTRASOUND FETAL MONITORING, MODELS FM10833 AND FM10834

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040819
510(k) Type
Traditional
Applicant
AMERICAN I.V. PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2004
Days to Decision
139 days
Submission Type
Summary