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

LISTERINE Sensitivity Defense Mouthrinse

K Number: K143155 · Decision Jan 29, 2015
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
1
Review Days
87

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LISTERINE Sensitivity Defense Mouthrinse
K Number
K143155
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Johnson & Johnson Healthcare Products, Division of Mcneil-Pp
Date Received
November 3, 2014
Decision Date
January 29, 2015
Product Code
LBH
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
LBH Varnish, Cavity

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LBH), ordered by most recent decision date.

View all