510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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R.H. Burton Co.

Grove City, OH, US

R.H. Burton Co. appears in FDA device records in Grove City, OH. FDA records list 19 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
19
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 19 510(k) clearances for R.H. Burton Co. between 1992 and 1993. The busiest year on record is 1993, with 17. The most recent is 1993, with 17.

Clearances by year, as a table
510(k) clearance decisions for R.H. Burton Co., by decision year
YearClearances
19922
199317
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K924773BURTON H- BASE TABLE - MODEL 1990HRXSubstantially Equivalent
K924786BURTON TRIAL LENS SETHPCSubstantially Equivalent
K924783BURTON SLIT LAMP - MODEL 850HJOSubstantially Equivalent
K924774BURTON AUTOMATIC PROJECTOR - MODEL CP-40HODSubstantially Equivalent
K924790BURTON AUTO REFRACTOR - MODEL BAR-7HKOSubstantially Equivalent
K924788BURTON LENSMETERHLMSubstantially Equivalent
K924785BURTON RADIUSGAUGE - MODEL 2030HLMSubstantially Equivalent
K924784BURTON PROJECTOR HEAD - MODEL 6000-HHOSSubstantially Equivalent
K924780BURTON OPHTHALMIC EXAM UNIT - MODEL 2201HMFSubstantially Equivalent
K924779BURTON KERATOMETER - MODLE 2040HJBSubstantially Equivalent
K924778BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8HKOSubstantially Equivalent
K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000HKXSubstantially Equivalent
K924776BURTON LENSMETER - MODEL 2021HLMSubstantially Equivalent
K924771BURTON OPHTHALMIC STAND - MODEL XL3200HMFSubstantially Equivalent
K924787BURTON SLIT LAMPHJOSubstantially Equivalent
K924782BURTON SLIT LAMP - MODEL 2000HJOSubstantially Equivalent
K924770BURTON HAND HELD SLIT LAMP - MODEL SL750HJOSubstantially Equivalent
K922242910T MONTORIZED INSTRUMENT TABLEHRJSubstantially Equivalent
K920571TRIAL LENS SETHPCSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain