Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K072402
Device Classification Name
Resin, Denture, Relining, Repairing, Rebasing
More FDA Info for this Device
510(K) Number
K072402
Device Name
Resin, Denture, Relining, Repairing, Rebasing
Applicant
CMP INDUSTRIES LLC.
413 NORTH PEARL ST.
ALBANY, NY 12207 US
Other 510(k) Applications for this Company
Contact
DEVON O HOWE
Other 510(k) Applications for this Contact
Regulation Number
872.3760
More FDA Info for this Regulation Number
Classification Product Code
EBI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/27/2007
Decision Date
10/19/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact