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DOPPLER FETAL HEARTBEAT RATE DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090510
510(k) Type
Traditional
Applicant
SHENZHEN BESTMAN INSTRUMENT CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/29/2010
Days to Decision
427 days
Submission Type
Summary

DOPPLER FETAL HEARTBEAT RATE DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090510
510(k) Type
Traditional
Applicant
SHENZHEN BESTMAN INSTRUMENT CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/29/2010
Days to Decision
427 days
Submission Type
Summary