UROSTYM— 510(k) K962009

Substantially Equivalent

Laborie Medical Technologies, Ltd.

FDA 510(k) clearance K962009 for UROSTYM, Substantially Equivalent on 1997-05-20. Applicant: Laborie Medical Technologies, Ltd..

Clearance details

Applicant: Laborie Medical Technologies, Ltd.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 1996-05-22
Decision date: 1997-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Burlington, VT, US

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