ECA CREAM REFORMULATION— 510(k) K801383

Name: FDA 510(k) clearance K801383
Creator: U.S. Food and Drug Administration
Published: 1980-06-17

Substantially Equivalent

Vanaray Laboratories, Inc.

FDA 510(k) clearance K801383 for ECA CREAM REFORMULATION, Substantially Equivalent on 1980-06-17. Applicant: Vanaray Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Vanaray Laboratories, Inc.
Product code: Code GYB
Device class: Class 2
Regulation: 21 CFR 882.1275
Advisory panel: Neurology
Date received: 1980-06-11
Decision date: 1980-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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