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

NIMETIC-DISPERS

K Number: K812119 · Decision Aug 31, 1981
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
10
Review Days
35

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Basic Information

Device Name
NIMETIC-DISPERS
K Number
K812119
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe-Premier Sales Co.
Date Received
July 27, 1981
Decision Date
August 31, 1981
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

Similar 510(k) Clearances

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

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Other Clearances by Espe-Premier Sales Co.

K Number Device Name
K812117 PERMAGUM ADHESIVE
K812116 PERMAGUM
K812115 KETAC-CHEM
K812118 NIMETIC POLISHING PASTE
K811624 VISIO-SEAL
K810266 ETCHING GEL
K810265 VISIO-BAND
K803227 VISIO-DISPERS
K803209 ELIPAR LIGHT SOURCE