RELIEF VALVE-HONAN INTRAOC. PRESSURE— 510(k) K820526

Name: FDA 510(k) clearance K820526
Creator: U.S. Food and Drug Administration
Published: 1982-03-25

Substantially Equivalent

The Lebanon Corp.

FDA 510(k) clearance K820526 for RELIEF VALVE-HONAN INTRAOC. PRESSURE, Substantially Equivalent on 1982-03-25. Applicant: The Lebanon Corp.. Device class: 2.

Clearance details

Applicant: The Lebanon Corp.
Product code: Code LCC
Device class: Class 2
Regulation: 21 CFR 886.4610
Advisory panel: Ophthalmic
Date received: 1982-02-26
Decision date: 1982-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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