UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES— 510(k) K993721

Substantially Equivalent

Laborie Medical Tech Corp.

FDA 510(k) clearance K993721 for UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES, Substantially Equivalent on 1999-11-29. Applicant: Laborie Medical Tech Corp..

Clearance details

Applicant: Laborie Medical Tech Corp.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 1999-11-03
Decision date: 1999-11-29
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Williston, VT, US

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