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FETAL MONITOR, MODELS BT-300 AND BT-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052190
510(k) Type
Traditional
Applicant
BISTOS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2005
Days to Decision
54 days
Submission Type
Summary

FETAL MONITOR, MODELS BT-300 AND BT-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052190
510(k) Type
Traditional
Applicant
BISTOS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2005
Days to Decision
54 days
Submission Type
Summary