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OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093600
510(k) Type
Traditional
Applicant
ACCELERATED CARE PLUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
14 days
Submission Type
Statement

OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093600
510(k) Type
Traditional
Applicant
ACCELERATED CARE PLUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
14 days
Submission Type
Statement