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

BENDA BRUSH

K Number: K885162 · Decision Jan 10, 1989
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
71
Applicant Total
47
Review Days
28

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Basic Information

Device Name
BENDA BRUSH
K Number
K885162
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Centrix, Inc.
Date Received
December 13, 1988
Decision Date
January 10, 1989
Product Code
EKJ
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
EKJ Burnisher, Operative

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K140144 BENDA WEDGE
K120176 SENZZZZZ AWAY
K111348 RE / STASIS (TM) GINGIVAL RETRACTION PASTE
K092384 LIQUICORD
K091380 CORDCAP
K021131 CHLORAPREP
K021146 D/SENSE 1-STEP
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