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

PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE

K Number: K994182 · Decision Feb 23, 2000
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
78
Review Days
75

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Basic Information

Device Name
PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE
K Number
K994182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pulpdent Corp.
Date Received
December 10, 1999
Decision Date
February 23, 2000
Product Code
LBH
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
LBH Varnish, Cavity

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Other Clearances by Pulpdent Corp.

K Number Device Name
K014133 PULPDENT NO-MIX ORTHODONTIC BRACKET ADHESIVE
K014138 PULPDENT TRIPLE-CURE REINFORCED GLASS IONOMER ORTHODONTIC CEMENT
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
K993683 PULPDENT UNO-DUO
K974202 PULPDENT CAVITY CLEANSER, PULPDENT CAVITY CLEANSER PLUS
K974398 PULPDENT CAVITY VARNISH
Search all 78 clearances from Pulpdent Corp. →