Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K100700
Device Classification Name
Tube, Feeding
More FDA Info for this Device
510(K) Number
K100700
Device Name
Tube, Feeding
Applicant
BENLAN, INC.
2760 BRIGHTON RD.
OAKVILLE, ONTARIO L6H 5T4 CA
Other 510(k) Applications for this Company
Contact
CHERYL BROWN
Other 510(k) Applications for this Contact
Regulation Number
876.5980
More FDA Info for this Regulation Number
Classification Product Code
FPD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/12/2010
Decision Date
12/13/2010
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact