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

PULPDENT DIAMOND POLISH

K Number: K911284 · Decision May 30, 1991
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
76
Applicant Total
78
Review Days
90

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Basic Information

Device Name
PULPDENT DIAMOND POLISH
K Number
K911284
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6030
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Pulpdent Corp.
Date Received
March 1, 1991
Decision Date
May 30, 1991
Product Code
EJR
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
EJR Agent, Polishing, Abrasive, Oral 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
K994182 PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE
K993683 PULPDENT UNO-DUO
K974202 PULPDENT CAVITY CLEANSER, PULPDENT CAVITY CLEANSER PLUS
Search all 78 clearances from Pulpdent Corp. →