BURTON KERATOMETER - MODLE 2040— 510(k) K924779

Name: FDA 510(k) clearance K924779
Creator: U.S. Food and Drug Administration
Published: 1993-04-05

Substantially Equivalent

R.H. Burton Co.

FDA 510(k) clearance K924779 for BURTON KERATOMETER - MODLE 2040, Substantially Equivalent on 1993-04-05. Applicant: R.H. Burton Co.. Device class: 1.

Clearance details

Applicant: R.H. Burton Co.
Product code: Code HJB
Device class: Class 1
Regulation: 21 CFR 886.1450
Advisory panel: Ophthalmic
Date received: 1992-09-23
Decision date: 1993-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grove City, OH, 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.