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

DEMETRON IDS CURING LIGHT

K Number: K042888 · Decision Nov 10, 2004
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
9
Review Days
22

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DEMETRON IDS CURING LIGHT
K Number
K042888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corp.
Date Received
October 19, 2004
Decision Date
November 10, 2004
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.

View all

Other Clearances by Kerr Corp.

K Number Device Name
K091613 TAKE 1
K090292 PREMISE MODIFIED
K081695 DMC COMPOSITE
K072622 STANDOUT 2
K031484 STAND OUT
K014179 DEMETRON LC
K010994 TAKE ONE BITE MODIFIED
K001655 PERMLASTIC 2