RODENSTOCK SCANNING LASER OPHTHALMOSCOPE— 510(k) K871268

Name: FDA 510(k) clearance K871268
Creator: U.S. Food and Drug Administration
Published: 1987-06-10

Substantially Equivalent

G. Rodenstock Instrumente GmbH

FDA 510(k) clearance K871268 for RODENSTOCK SCANNING LASER OPHTHALMOSCOPE, Substantially Equivalent on 1987-06-10. Applicant: G. Rodenstock Instrumente GmbH. Device class: 2.

Clearance details

Applicant: G. Rodenstock Instrumente GmbH
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1987-03-31
Decision date: 1987-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Munchen 70, West Germany, DE

Download summary PDF View on FDA.gov ↗

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