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

NEUTRASAL

K Number: K091718 · Decision Sep 2, 2009
Classifications
1
FEI Numbers
39
Registration Numbers
40
Same Product Code
49
Applicant Total
1
Review Days
83

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Basic Information

Device Name
NEUTRASAL
K Number
K091718
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bartor Pharmacal Co., Inc.
Date Received
June 11, 2009
Decision Date
September 2, 2009
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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