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

OPTIBOND

K Number: K940513 · Decision Apr 15, 1994
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
32
Review Days
70

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
OPTIBOND
K Number
K940513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corporation (Danbury)
Date Received
February 4, 1994
Decision Date
April 15, 1994
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

Similar 510(k) Clearances

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

View all

Other Clearances by Kerr Corporation (Danbury)

K Number Device Name
K051545 L.E. DEMETRON II
K020091 OPTILUX 501
K951663 TYTIN R
K951511 TYTIN ADMIX
K942480 M4 CONTRA-ANGLE HANDPIECE
K935535 TYTIN
K934690 KERR OPTIBOND, MODIFICATION
K923546 OPTIBOND
K915847 AUTOMIX DENTAL AMALGAMATOR
K904756 MATRICS
Search all 32 clearances from Kerr Corporation (Danbury) →