AQUALUX LENS CASE— 510(k) K862811

Name: FDA 510(k) clearance K862811
Creator: U.S. Food and Drug Administration
Published: 1986-09-03

Substantially Equivalent

Safeway Products, Inc.

FDA 510(k) clearance K862811 for AQUALUX LENS CASE, Substantially Equivalent on 1986-09-03. Applicant: Safeway Products, Inc.. Device class: Unclassified.

Clearance details

Applicant: Safeway Products, Inc.
Product code: Code HPX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1986-07-24
Decision date: 1986-09-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Middletown, CT, US

Download summary PDF View on FDA.gov ↗

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