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

INTERFACE - CAVITY LINER

K Number: K897130 · Decision Mar 27, 1990
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
72
Review Days
90

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Basic Information

Device Name
INTERFACE - CAVITY LINER
K Number
K897130
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Scientific Pharmaceuticals, Inc.
Date Received
December 27, 1989
Decision Date
March 27, 1990
Product Code
EJK
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
EJK Liner, Cavity, Calcium Hydroxide

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K Number Device Name
K051952 EUGENONE
K041886 PROVISO
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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. →