Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K071845
Device Classification Name
Cannula, Sinus
More FDA Info for this Device
510(K) Number
K071845
Device Name
Cannula, Sinus
Applicant
ACCLARENT, INC.
1525-B O'BRIEN DR.
MENLO PARK, CA 94025 US
Other 510(k) Applications for this Company
Contact
KERI YEN
Other 510(k) Applications for this Contact
Regulation Number
878.4800
More FDA Info for this Regulation Number
Classification Product Code
KAM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/05/2007
Decision Date
09/28/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact