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

ANTERIOR/POSTERIOR RESTORATIVE, BOND

K Number: K791078 · Decision Aug 10, 1979
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
51
Applicant Total
72
Review Days
59

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Basic Information

Device Name
ANTERIOR/POSTERIOR RESTORATIVE, BOND
K Number
K791078
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3310
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Scientific Pharmaceuticals, Inc.
Date Received
June 12, 1979
Decision Date
August 10, 1979
Product Code
EBD
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
EBD Coating, Filling Material, Resin

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Other Clearances by Scientific Pharmaceuticals, Inc.

K Number Device Name
K051952 EUGENONE
K041886 PROVISO
K013555 SCI-PHARM POST SECURE
K001446 LIGHT-CURED ORTHODONTIC BAND CEMENT
K993324 CARBOCEM ZINC POLYCARBOXYLATE CEMENT
K982915 SCI-PHARM DFV VARNISH
K983305 SCI-PHARM DESENSITIZING VARNISH
K982913 ZINFOS ZINC PHOSPHATE CEMENT
K944466 SEALDENT
K930584 MAGNACORE
Search all 72 clearances from Scientific Pharmaceuticals, Inc. →