FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

THE TOOTHPIK

K Number: K830225 · Decision Feb 18, 1983
Classifications
1
FEI Numbers
335
Registration Numbers
336
Same Product Code
61
Applicant Total
1
Review Days
25

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Basic Information

Device Name
THE TOOTHPIK
K Number
K830225
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6390
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Fred M. Davis
Date Received
January 24, 1983
Decision Date
February 18, 1983
Product Code
JES
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
JES Floss, Dental

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