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R.H. Burton Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K924773BURTON H- BASE TABLE - MODEL 1990June 7, 1993
K924786BURTON TRIAL LENS SETApril 14, 1993
K924774BURTON AUTOMATIC PROJECTOR - MODEL CP-40April 14, 1993
K924783BURTON SLIT LAMP - MODEL 850April 14, 1993
K924779BURTON KERATOMETER - MODLE 2040April 5, 1993
K924785BURTON RADIUSGAUGE - MODEL 2030April 5, 1993
K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000April 5, 1993
K924776BURTON LENSMETER - MODEL 2021April 5, 1993
K924788BURTON LENSMETERApril 5, 1993
K924780BURTON OPHTHALMIC EXAM UNIT - MODEL 2201April 5, 1993
K924784BURTON PROJECTOR HEAD - MODEL 6000-HApril 5, 1993
K924771BURTON OPHTHALMIC STAND - MODEL XL3200April 5, 1993
K924790BURTON AUTO REFRACTOR - MODEL BAR-7April 5, 1993
K924778BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8April 5, 1993
K924770BURTON HAND HELD SLIT LAMP - MODEL SL750January 27, 1993
K924782BURTON SLIT LAMP - MODEL 2000January 27, 1993
K924787BURTON SLIT LAMPJanuary 27, 1993
K922242910T MONTORIZED INSTRUMENT TABLESeptember 30, 1992
K920571TRIAL LENS SETMay 7, 1992