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BIOSYS FETAL MONITOR, MODEL IFM-500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994008
510(k) Type
Traditional
Applicant
BIOSYS CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2000
Days to Decision
310 days
Submission Type
Summary

BIOSYS FETAL MONITOR, MODEL IFM-500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994008
510(k) Type
Traditional
Applicant
BIOSYS CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2000
Days to Decision
310 days
Submission Type
Summary