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INNOVA RECTAL STIMULATON ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954272
510(k) Type
Traditional
Applicant
EMPI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
216 days
Submission Type
Summary

INNOVA RECTAL STIMULATON ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954272
510(k) Type
Traditional
Applicant
EMPI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
216 days
Submission Type
Summary