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

Dentilube Spray

K Number: K202689 · Decision Sep 3, 2021
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
48
Applicant Total
1
Review Days
353

Basic Information

Device Name
Dentilube Spray
K Number
K202689
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oxy2plus, LLC
Date Received
September 15, 2020
Decision Date
September 3, 2021
Product Code
LFD
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
LFD Saliva, Artificial

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