510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924788Substantially Equivalent

Burton Lensmeter

R.H. Burton Co., Grove City OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924788 is the FDA 510(k) clearance record for BURTON LENSMETER, a class I device, cleared for R.H. Burton Co. on under FDA product code HLM (Instrument, Measuring, Lens, Ac-Powered). FDA records list 19 510(k) clearances for R.H. Burton Co., from to . As of , FDA records show no recalls naming K924788.

Clearance record

Decision date
Received
(194 days to decision)
Product code
HLM Instrument, Measuring, Lens, Ac-Powered
Regulation
21 CFR 886.1425
Device class
Class I
Review panel
Ophthalmic
Applicant
R.H. Burton Co. 3965 Brookham Dr., Grove City OH
510(k) summary
Statement
Third party review
No

Clearances, product code HLM

Trailing 12 months

FDA records hold no clearances under product code HLM in the trailing twelve months.

FDA records show no clearances under product code HLM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HLM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260