BURTON AUTO REFRACTOR - MODEL BAR-7— 510(k) K924790

Name: FDA 510(k) clearance K924790
Creator: U.S. Food and Drug Administration
Published: 1993-04-05

Substantially Equivalent

R.H. Burton Co.

FDA 510(k) clearance K924790 for BURTON AUTO REFRACTOR - MODEL BAR-7, Substantially Equivalent on 1993-04-05. Applicant: R.H. Burton Co.. Device class: 1.

Clearance details

Applicant: R.H. Burton Co.
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
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 ↗

Recent devices under product code HKO

view all

K031831 — TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM2003-12-19
K000327 — WAVESCAN WAVEFRONT SYSTEM MODEL HS 12000-05-02
K951179 — DIGITAL RETINOSCOPIC PHOTOMETER1995-05-30
K945959 — VIDEO VISION ANALYZER (VIVA), VRB 1001995-03-01
K942242 — AUTO REF-KERATOMETER, RK-31994-09-02

More clearances from R.H. Burton Co.

view all

K924773 — BURTON H- BASE TABLE - MODEL 19901993-06-07
K924774 — BURTON AUTOMATIC PROJECTOR - MODEL CP-401993-04-14
K924783 — BURTON SLIT LAMP - MODEL 8501993-04-14
K924786 — BURTON TRIAL LENS SET1993-04-14
K924771 — BURTON OPHTHALMIC STAND - MODEL XL32001993-04-05

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