Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K060186
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K060186
Device Name
Anesthesia Conduction Kit
Applicant
TE ME NA SAS
962 ALLEGRO LANE
APOLLO BEACH, FL 33572 US
Other 510(k) Applications for this Company
Contact
ARTHUR WARD
Other 510(k) Applications for this Contact
Regulation Number
868.5140
More FDA Info for this Regulation Number
Classification Product Code
CAZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/24/2006
Decision Date
07/18/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact