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CADENCE, CADENCE DUAL, CADENCE II FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082369
510(k) Type
Special
Applicant
EDAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2008
Days to Decision
81 days
Submission Type
Summary

CADENCE, CADENCE DUAL, CADENCE II FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082369
510(k) Type
Special
Applicant
EDAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2008
Days to Decision
81 days
Submission Type
Summary