FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LIGHT CURE DENTIN AND LINER BASE PRODUCT LINE

K Number: K921408 · Decision Nov 24, 1992
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
103
Review Days
245

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Basic Information

Device Name
LIGHT CURE DENTIN AND LINER BASE PRODUCT LINE
K Number
K921408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ultradent Products, Inc.
Date Received
March 24, 1992
Decision Date
November 24, 1992
Product Code
EJK
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
EJK Liner, Cavity, Calcium Hydroxide

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