TRIAL LENS SET— 510(k) K920571

Substantially Equivalent

R.H. Burton Co.

FDA 510(k) clearance K920571 for TRIAL LENS SET, Substantially Equivalent on 1992-05-07. Applicant: R.H. Burton Co.. Device class: 1.

Clearance details

Applicant: R.H. Burton Co.
Product code: Code HPC
Device class: Class 1
Regulation: 21 CFR 886.1405
Advisory panel: Ophthalmic
Date received: 1992-02-07
Decision date: 1992-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grove City, OH, US

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