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FDA 510(k), K102330, AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
FDA 510(k), K102330, AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
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510(K) Number: K102330
Device Name: AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
Manufacturer: STERIS Corporation
Device Classification Name: sterilizer, chemical
Regulation Number: 880.6860
Classification Product Code: MLR
Date Received: 08/17/2010
Decision Date: 08/12/2011
Regulation Medical Specialty: General Hospital
Device Name: AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
Manufacturer: STERIS Corporation
Device Classification Name: sterilizer, chemical
Regulation Number: 880.6860
Classification Product Code: MLR
Date Received: 08/17/2010
Decision Date: 08/12/2011
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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