Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K090135
Device Classification Name
More FDA Info for this Device
510(K) Number
K090135
Device Name
TRIMIRA IDENTAFI 3000
Applicant
REMICALM, LLC
952 ECHO LANE, SUITE 333
HOUSTON, TX 77024-2758 US
Other 510(k) Applications for this Company
Contact
DAVID B JONES
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
NXV
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/21/2009
Decision Date
02/17/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact