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510(k) K951113

CROSS-CHECKS by Steritec Products Mfg Co, Inc. — Product Code LRT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1996
Date Received
March 10, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Indicator, Sterilization
Device Class
Class II
Regulation Number
880.2800
Review Panel
HO
Submission Type

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