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UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070331
510(k) Type
Traditional
Applicant
LABORIE MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2007
Days to Decision
88 days
Submission Type
Statement

UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070331
510(k) Type
Traditional
Applicant
LABORIE MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2007
Days to Decision
88 days
Submission Type
Statement