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

AMERICAN DENTAL PRODUCTS HG 35 DESENSITIZER WITH FLUORIDE

K Number: K964133 · Decision Jan 9, 1997
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
23
Review Days
86

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Basic Information

Device Name
AMERICAN DENTAL PRODUCTS HG 35 DESENSITIZER WITH FLUORIDE
K Number
K964133
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
American Dental Products, Inc.
Date Received
October 15, 1996
Decision Date
January 9, 1997
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

Similar 510(k) Clearances

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Other Clearances by American Dental Products, Inc.

K Number Device Name
K093014 AMERICAN DENTAL PRODUCTS SE BONDEASY
K994368 AMERICAN DENTAL PRODUCTS CARIES-DETECTOR PLUS
K991099 AMERICAN DENTAL PRODUCTS ETCH-DETECT
K973185 AMERICAN DENTAL PRODUCTS HB-35 DESENSITIZER WITH FLUORIDE
K954637 AMERICAN DENTAL PRODUCTS TISSUE CONDITIONER & TEMPORARY RELINER
K954876 AMERICAN DENTAL PRODUCTS ROOT CANAL SEALER, WACH'S FORMULA
K954406 AMERICAN DENTAL PRODUCTS COMPOSITE RESIN CORE PASTE WITH FLUORIDE
K954701 AMERICAN DENTAL PRODUCTS PIT & FISSUE SEALANT LIGHT CURING
K954407 AMERICAN DENTAL PRODUCTS WHITE COMPOSITE RESIN CORE PASTE WITH FLUORIDE
K954408 AMERICAN DENTAL PRODUCTS LIGHT ACTIVATED COMPOSITE RESIN CORE BUILDUP BLUE PASTEE
Search all 23 clearances from American Dental Products, Inc. →