DURALITE LENS— 510(k) K800192

Name: FDA 510(k) clearance K800192
Creator: U.S. Food and Drug Administration
Published: 1980-03-12

Substantially Equivalent

American Optical Corp.

FDA 510(k) clearance K800192 for DURALITE LENS, Substantially Equivalent on 1980-03-12. Applicant: American Optical Corp.. Device class: Unclassified.

Clearance details

Applicant: American Optical Corp.
Product code: Code HPX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1980-01-29
Decision date: 1980-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K931357 — AOD4000 DISPOSABLE PAK1994-01-25

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