BURTON OPHTHALMIC EXAM UNIT - MODEL 2201— 510(k) K924780

Name: FDA 510(k) clearance K924780
Creator: U.S. Food and Drug Administration
Published: 1993-04-05

Substantially Equivalent

R.H. Burton Co.

FDA 510(k) clearance K924780 for BURTON OPHTHALMIC EXAM UNIT - MODEL 2201, Substantially Equivalent on 1993-04-05. Applicant: R.H. Burton Co.. Device class: 1.

Clearance details

Applicant: R.H. Burton Co.
Product code: Code HMF
Device class: Class 1
Regulation: 21 CFR 886.1860
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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