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FDA 510(k) Application Details - K041149
Device Classification Name
System, Imaging, Esophageal, Wireless, Capsule
More FDA Info for this Device
510(K) Number
K041149
Device Name
System, Imaging, Esophageal, Wireless, Capsule
Applicant
GIVEN IMAGING LTD.
13 HAYETZIRA STREET
NEW INDUSTRIAL ZONE
YOKNEAM 20692 IL
Other 510(k) Applications for this Company
Contact
SHOSH FRIEDMAN
Other 510(k) Applications for this Contact
Regulation Number
876.1300
More FDA Info for this Regulation Number
Classification Product Code
NSI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/03/2004
Decision Date
10/25/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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