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FDA 510(k), K923739, ABTOX SERILIZATION PROCESS BIOLOGICAL INDICATOR
FDA 510(k), K923739, ABTOX SERILIZATION PROCESS BIOLOGICAL INDICATOR
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510(K) Number: K923739
Device Name: ABTOX SERILIZATION PROCESS BIOLOGICAL INDICATOR
Manufacturer: ABTOX, INC.
Device Classification Name: indicator, biological sterilization process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 07/27/1992
Decision Date: 12/22/1994
Regulation Medical Specialty: General Hospital
Device Name: ABTOX SERILIZATION PROCESS BIOLOGICAL INDICATOR
Manufacturer: ABTOX, INC.
Device Classification Name: indicator, biological sterilization process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 07/27/1992
Decision Date: 12/22/1994
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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