FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PL EXAM LIGHT

K Number: K860088 · Decision Jan 24, 1986
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
28
Applicant Total
15
Review Days
14

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Basic Information

Device Name
PL EXAM LIGHT
K Number
K860088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Burton Medical Products Corp.
Date Received
January 10, 1986
Decision Date
January 24, 1986
Product Code
FTD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FTD Lamp, Surgical

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K963682 GENIE' SINGLE CEILING AND DOUBLE CEILING
K961843 GENIE
K935102 SATURN LIGHT
K942553 GENESIS
K936088 WAVE FLUORESCENT MAGNIFIER
K931645 HALUX TASKLIGHT
K901706 LIGHT, HEAD, EXAMINATION
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