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FDA 510(k), K063159, STERILOX LIQUID CHEMICAL STERILANT SYSTEM
FDA 510(k), K063159, STERILOX LIQUID CHEMICAL STERILANT SYSTEM
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510(K) Number: K063159
Device Name: STERILOX LIQUID CHEMICAL STERILANT SYSTEM
Manufacturer: HOWARD MANN
Device Classification Name: Sterilant, Medical Devices
Regulation Number: MED
Classification Product Code: 10/17/2006
Date Received: 04/02/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERILOX LIQUID CHEMICAL STERILANT SYSTEM
Manufacturer: HOWARD MANN
Device Classification Name: Sterilant, Medical Devices
Regulation Number: MED
Classification Product Code: 10/17/2006
Date Received: 04/02/2007
Decision Date: Substantially Equivalent (SESE)
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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