FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

PULPDENT SODIUM HYPOCHLORITE SOLUTION

K Number: K962743 · Decision Aug 6, 1996
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
40
Applicant Total
78
Review Days
22

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Basic Information

Device Name
PULPDENT SODIUM HYPOCHLORITE SOLUTION
K Number
K962743
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pulpdent Corp.
Date Received
July 15, 1996
Decision Date
August 6, 1996
Product Code
KJJ
Advisory Committee
Unknown
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
KJJ Cleanser, Root Canal

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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. →