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

LIGHT-PAK

K Number: K791733 · Decision Oct 23, 1979
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
17
Applicant Total
13
Review Days
56

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Basic Information

Device Name
LIGHT-PAK
K Number
K791733
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4620
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Midwest
Date Received
August 28, 1979
Decision Date
October 23, 1979
Product Code
EAY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EAY Light, Fiber Optic, Dental

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K792304 MW-8000
K792302 LS-100
K792303 MW 8000-I
K791771 ORALUMINATOR III AUTO-LIGHT
K790113 MIDWEST 1000
K781878 LIGHT, INSIDE
K760794 FIBER OPTICS HIGH SPEED HANDPIECE
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