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FDA 510(k) Application Details - K112791
Device Classification Name
Pad, Alcohol, Device Disinfectant
More FDA Info for this Device
510(K) Number
K112791
Device Name
Pad, Alcohol, Device Disinfectant
Applicant
CR BARD
605 NORTH 5600 WEST
SALT LAKE CITY, UT 84116 US
Other 510(k) Applications for this Company
Contact
LYNN M KIRCHOFF
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LKB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/26/2011
Decision Date
02/24/2012
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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