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

DENTOLOCK DENTURE ADHESIVE CREAM

K Number: K831265 · Decision May 9, 1983
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
3
Applicant Total
6
Review Days
21

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Basic Information

Device Name
DENTOLOCK DENTURE ADHESIVE CREAM
K Number
K831265
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3410
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Solar Dental Co., Inc.
Date Received
April 18, 1983
Decision Date
May 9, 1983
Product Code
KOQ
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
KOQ Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KOQ), ordered by most recent decision date.

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Other Clearances by Solar Dental Co., Inc.

K Number Device Name
K871980 D-23 DENTURE ADHESIVE
K861846 HYDRON ROOT CANAL FILLING & MARK IV STARTER KIT
K852926 DENTOLOCK II DENTURE ADHESIVE CREAM
K831294 SOLARCRY/TEMPORARY CROWN & BRIDGE MAT
K831293 SOLARCRYL CUSTOM TRAY MATERIAL