Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K090479
Device Classification Name
Analyzer, Body Composition
More FDA Info for this Device
510(K) Number
K090479
Device Name
Analyzer, Body Composition
Applicant
TANITA CORPORATION OF AMERICA
2625 SOUTH CLEARBROOK DRIVE
ARLINGTON HEIGHTS, IL 60005 US
Other 510(k) Applications for this Company
Contact
TOSHIHIKO ISHIKAWA
Other 510(k) Applications for this Contact
Regulation Number
870.2770
More FDA Info for this Regulation Number
Classification Product Code
MNW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/24/2009
Decision Date
07/07/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
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