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

NIMETIC-DISPERS

K Number: K802049 · Decision Sep 16, 1980
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
8
Review Days
22

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Basic Information

Device Name
NIMETIC-DISPERS
K Number
K802049
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe Dental Products
Date Received
August 25, 1980
Decision Date
September 16, 1980
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by Espe Dental Products

K Number Device Name
K810950 VISIO-SEAL
K802819 KETAC-CEM IN REF. TO K802048
K800031 PERMADYNE POLYETHER RUBBER IMPRESSION
K771889 UNIOLITE
K771901 CAPMIX
K771120 IMPREFLEX ALGINATE IMPRESSION MATERIAL
K771119 PASTES, RESTORATIVE & TINTED, DEBTAL