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INNOVA RECTAL STIMULATON ELECTRODE

Page Type
Cleared 510(K)
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)
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