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FDA 510(k) Application Details - K992744
Device Classification Name
Sterilizer, Steam
More FDA Info for this Device
510(K) Number
K992744
Device Name
Sterilizer, Steam
Applicant
MIDMARK CORP.
60 VISTA DR.
P.O. BOX 286
VERSAILLES, OH 45380 US
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Contact
MIKE SNYDER
Other 510(k) Applications for this Contact
Regulation Number
880.6880
More FDA Info for this Regulation Number
Classification Product Code
FLE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/16/1999
Decision Date
01/10/2000
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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