FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BURTON KERATOMETER - MODLE 2040

K Number: K924779 · Decision Apr 5, 1993
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
4
Applicant Total
19
Review Days
194

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Basic Information

Device Name
BURTON KERATOMETER - MODLE 2040
K Number
K924779
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1450
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
R.H. Burton Co.
Date Received
September 23, 1992
Decision Date
April 5, 1993
Product Code
HJB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HJB Instrument, Measuring, Corneal Radius

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HJB), ordered by most recent decision date.

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Other Clearances by R.H. Burton Co.

K Number Device Name
K924773 BURTON H- BASE TABLE - MODEL 1990
K924783 BURTON SLIT LAMP - MODEL 850
K924774 BURTON AUTOMATIC PROJECTOR - MODEL CP-40
K924786 BURTON TRIAL LENS SET
K924776 BURTON LENSMETER - MODEL 2021
K924780 BURTON OPHTHALMIC EXAM UNIT - MODEL 2201
K924788 BURTON LENSMETER
K924785 BURTON RADIUSGAUGE - MODEL 2030
K924790 BURTON AUTO REFRACTOR - MODEL BAR-7
K924777 BURTON APPLANATION TONOMETER - MODEL T850 & T1000
Search all 19 clearances from R.H. Burton Co. →