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

ELIPAR LIGHT SOURCE

K Number: K803209 · Decision Jan 14, 1981
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
10
Review Days
27

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Basic Information

Device Name
ELIPAR LIGHT SOURCE
K Number
K803209
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe-Premier Sales Co.
Date Received
December 18, 1980
Decision Date
January 14, 1981
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EBZ), 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
K812119 NIMETIC-DISPERS
K811624 VISIO-SEAL
K810266 ETCHING GEL
K810265 VISIO-BAND
K803227 VISIO-DISPERS