ALCON INDIRECT OPHTHALMOSCOPE— 510(k) K822104

Name: FDA 510(k) clearance K822104
Creator: U.S. Food and Drug Administration
Published: 1982-08-10

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K822104 for ALCON INDIRECT OPHTHALMOSCOPE, Substantially Equivalent on 1982-08-10. Applicant: Alcon Laboratories. Device class: 2.

Clearance details

Applicant: Alcon Laboratories
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1982-07-19
Decision date: 1982-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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