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FDA 510(k) Application Details - K072634
Device Classification Name
Compressor, Air, Portable
More FDA Info for this Device
510(K) Number
K072634
Device Name
Compressor, Air, Portable
Applicant
EMG TECHNOLOGY CO., LTD.
4F-2, NO. 210, 38 RD.
TAICHUNG INDUSTRIAL PARK
SHITUEN CHIU, TAICHUNG 40768 TW
Other 510(k) Applications for this Company
Contact
SALLY CHUANG
Other 510(k) Applications for this Contact
Regulation Number
868.6250
More FDA Info for this Regulation Number
Classification Product Code
BTI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/18/2007
Decision Date
11/19/2008
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
Y
Expedited Review
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