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PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993976
510(k) Type
Traditional
Applicant
The Prometheus Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2000
Days to Decision
90 days
Submission Type
Summary

PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993976
510(k) Type
Traditional
Applicant
The Prometheus Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2000
Days to Decision
90 days
Submission Type
Summary