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

BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH

K Number: K101477 · Decision Sep 28, 2010
Classifications
1
FEI Numbers
39
Registration Numbers
40
Same Product Code
49
Applicant Total
3
Review Days
123

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
BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH
K Number
K101477
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Glaxosmithkline Consumer Healthcare (Gskch)
Date Received
May 28, 2010
Decision Date
September 28, 2010
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

Similar 510(k) Clearances

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

View all

Other Clearances by Glaxosmithkline Consumer Healthcare (Gskch)

K Number Device Name
K123731 BIOTENE ORAL BALANCE GEL, BIOTENE DRY MOUTH ORAL RINSE, BIOTENE MOISTURIZING MOUTH SPRAY
K103745 BIOTENE MOISTURIZING MOUTH SPRAY FOR DRY MOUTH SYMPTOM RELIEF