RODENSTOCK SCANNING LASER OPHTHALMOSCOPE— 510(k) K882517

Name: FDA 510(k) clearance K882517
Creator: U.S. Food and Drug Administration
Published: 1989-01-24

Substantially Equivalent

Rodenstock Instrument Corp.

FDA 510(k) clearance K882517 for RODENSTOCK SCANNING LASER OPHTHALMOSCOPE, Substantially Equivalent on 1989-01-24. Applicant: Rodenstock Instrument Corp.. Device class: 2.

Clearance details

Applicant: Rodenstock Instrument Corp.
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1988-06-17
Decision date: 1989-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

Download summary PDF View on FDA.gov ↗

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