UROSTYM BIOFEEDBACK AND STIMULATION PROBES— 510(k) K990041

Substantially Equivalent

Laborie Medical Tech Corp.

FDA 510(k) clearance K990041 for UROSTYM BIOFEEDBACK AND STIMULATION PROBES, Substantially Equivalent on 1999-08-05. Applicant: Laborie Medical Tech Corp..

Clearance details

Applicant: Laborie Medical Tech Corp.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 1999-01-06
Decision date: 1999-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Williston, VT, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.