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FDA 510(k) Application Details - K972300
Device Classification Name
Indicator, Physical/Chemical Sterilization Process
More FDA Info for this Device
510(K) Number
K972300
Device Name
Indicator, Physical/Chemical Sterilization Process
Applicant
STERITEC PRODUCTS MFG. CO., INC.
680 ATCHISON WAY
SUITE 600
CASTLE ROCK, CO 80104 US
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Contact
TOM ROLL
Other 510(k) Applications for this Contact
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
06/19/1997
Decision Date
03/25/1998
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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