LIQUID LIGHT 500— 510(k) K940962

Substantially Equivalent

Incredivision, Inc.

FDA 510(k) clearance K940962 for LIQUID LIGHT 500, Substantially Equivalent on 1994-04-08. Applicant: Incredivision, Inc..

Clearance details

Applicant: Incredivision, Inc.
Product code: Code FFS
Advisory panel: Gastroenterology, Urology
Date received: 1994-03-02
Decision date: 1994-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wellesley, MA, US

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