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

BURTON RADIUSGAUGE - MODEL 2030

K Number: K924785 · Decision Apr 5, 1993
Classifications
1
FEI Numbers
68
Registration Numbers
69
Same Product Code
15
Applicant Total
19
Review Days
194

Basic Information

Device Name
BURTON RADIUSGAUGE - MODEL 2030
K Number
K924785
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1425
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
HLM
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
HLM Instrument, Measuring, Lens, Ac-Powered

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