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

RITTER MODEL 158 AND 159 EXAM LIGHTS

K Number: K932719 · Decision Dec 2, 1993
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
31
Review Days
181

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Basic Information

Device Name
RITTER MODEL 158 AND 159 EXAM LIGHTS
K Number
K932719
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Midmark Corp.
Date Received
June 4, 1993
Decision Date
December 2, 1993
Product Code
KZF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KZF Device, Medical Examination, Ac Powered

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