AML (ANGLE MAGNIFYING LENS— 510(k) K823719

Substantially Equivalent

Nikon, Inc.

FDA 510(k) clearance K823719 for AML (ANGLE MAGNIFYING LENS, Substantially Equivalent on 1983-01-05. Applicant: Nikon, Inc.. Device class: 2.

Clearance details

Applicant: Nikon, Inc.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1982-12-10
Decision date: 1983-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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