Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K072342
Device Classification Name
Varnish, Cavity
More FDA Info for this Device
510(K) Number
K072342
Device Name
Varnish, Cavity
Applicant
DENTSPLY INTERNATIONAL, INC.
SUSQUEHANNA COMMERCE CTR., 221
W. PHILADELPHIA ST., SUITE 60
YORK, PA 17404 US
Other 510(k) Applications for this Company
Contact
HELEN LEWIS
Other 510(k) Applications for this Contact
Regulation Number
872.3260
More FDA Info for this Regulation Number
Classification Product Code
LBH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/21/2007
Decision Date
10/03/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact