Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K122721
Device Classification Name
Cuff, Tracheal Tube, Inflatable
More FDA Info for this Device
510(K) Number
K122721
Device Name
Cuff, Tracheal Tube, Inflatable
Applicant
HOSPITECH RESPIRATION LTD.
31 HAAVODA ST
BINYAMINA 30500 IL
Other 510(k) Applications for this Company
Contact
YORAM LEVY
Other 510(k) Applications for this Contact
Regulation Number
868.5750
More FDA Info for this Regulation Number
Classification Product Code
BSK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/05/2012
Decision Date
05/03/2013
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