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UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993721
510(k) Type
Abbreviated
Applicant
LABORIE MEDICAL TECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1999
Days to Decision
26 days
Submission Type
Statement

UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993721
510(k) Type
Abbreviated
Applicant
LABORIE MEDICAL TECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1999
Days to Decision
26 days
Submission Type
Statement