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FDA 510(k) Application Details - K020589
Device Classification Name
Indicator, Physical/Chemical Sterilization Process
More FDA Info for this Device
510(K) Number
K020589
Device Name
Indicator, Physical/Chemical Sterilization Process
Applicant
3M COMPANY
3M CENTER, BLDG. 275-5W-06
ST. PAUL, MN 55133-3275 US
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Contact
JOANN L HUEHN
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Regulation Number
880.2800
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Classification Product Code
JOJ
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More FDA Info for this Product Code
Date Received
02/22/2002
Decision Date
04/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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