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FDA 510(k) Application Details - K092327
Device Classification Name
Polymer Patient Examination Glove
More FDA Info for this Device
510(K) Number
K092327
Device Name
Polymer Patient Examination Glove
Applicant
ANSELL HEALTHCARE PRODUCTS LLC
1635 INDUSTRIAL RD.
DOTHAN, AL 36303 US
Other 510(k) Applications for this Company
Contact
CYNTHIA A INGRAM
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZA
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More FDA Info for this Product Code
Date Received
08/04/2009
Decision Date
09/21/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
Y
Expedited Review
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