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FM-9000 PLUS FETAL AND MATERNAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112317
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2011
Days to Decision
132 days
Submission Type
Summary

FM-9000 PLUS FETAL AND MATERNAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112317
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2011
Days to Decision
132 days
Submission Type
Summary