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

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

K Number: K910610 · Decision Jul 9, 1991
Classifications
1
FEI Numbers
343
Registration Numbers
344
Same Product Code
53
Applicant Total
92
Review Days
147

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Basic Information

Device Name
INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT
K Number
K910610
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6865
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Bausch & Lomb, Inc.
Date Received
February 12, 1991
Decision Date
July 9, 1991
Product Code
JEQ
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
JEQ Toothbrush, Powered

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