FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

LunaGuard Nighttime Dental Protector

K Number: K191033 · Decision Aug 5, 2019
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
44
Applicant Total
1
Review Days
109

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Basic Information

Device Name
LunaGuard Nighttime Dental Protector
K Number
K191033
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mckeon Products
Date Received
April 18, 2019
Decision Date
August 5, 2019
Product Code
OBR
Advisory Committee
Unknown
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
OBR Mouthguard, Over-The-Counter

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