Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K013865
Device Classification Name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
More FDA Info for this Device
510(K) Number
K013865
Device Name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Applicant
COOK, INC.
925 SOUTH CURRY PIKE
P.O. BOX 489
BLOOMINGTON, IN 47402 US
Other 510(k) Applications for this Company
Contact
LISA HOPKINS
Other 510(k) Applications for this Contact
Regulation Number
868.5740
More FDA Info for this Regulation Number
Classification Product Code
CBI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/21/2001
Decision Date
04/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact