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

MIRROR SHIELD

K Number: K901053 · Decision May 7, 1990
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
71
Applicant Total
78
Review Days
63

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Basic Information

Device Name
MIRROR SHIELD
K Number
K901053
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Pulpdent Corp.
Date Received
March 5, 1990
Decision Date
May 7, 1990
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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K Number Device Name
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K020115 PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM
K014059 PULPDENT TRANS OBA ORTHODONTIC BRACKET ADHESIVE
K013411 PULPDENT CAVITY PREPARATION IV
K994180 PULPDENT CAVITY PREPARATION III
K994181 PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE
K994182 PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE
K993683 PULPDENT UNO-DUO
K974202 PULPDENT CAVITY CLEANSER, PULPDENT CAVITY CLEANSER PLUS
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