D.L. SCOPE OPHTHALMOSCOPE— 510(k) K896072

Name: FDA 510(k) clearance K896072
Creator: U.S. Food and Drug Administration
Published: 1989-11-27

Substantially Equivalent

North American Medical Products, Inc.

FDA 510(k) clearance K896072 for D.L. SCOPE OPHTHALMOSCOPE, Substantially Equivalent on 1989-11-27. Applicant: North American Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: North American Medical Products, Inc.
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1989-10-19
Decision date: 1989-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Loudonville, NY, US

Download summary PDF View on FDA.gov ↗

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