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.. Device class: 2.

Clearance details

Applicant: Incredivision, Inc.
Product code: Code FFS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1994-03-02
Decision date: 1994-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wellesley, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Incredivision, Inc.

K940963 — XENON LIGHT SOURCE1994-04-08

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