BURTON LENSMETER— 510(k) K924788

Substantially Equivalent

R.H. Burton Co.

FDA 510(k) clearance K924788 for BURTON LENSMETER, Substantially Equivalent on 1993-04-05. Applicant: R.H. Burton Co..

Clearance details

Applicant
R.H. Burton Co.
Product code
Code HLM
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Grove City, OH, US
Download summary PDFView on FDA.gov ↗

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