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FDA 510(k), K092622, STERRAD 100NX STERILIZER EXPRESS CYCLE
FDA 510(k), K092622, STERRAD 100NX STERILIZER EXPRESS CYCLE
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510(K) Number: K092622
Device Name: STERRAD 100NX STERILIZER EXPRESS CYCLE
Manufacturer: ADVANCED STERILIZATION PRODUCTS
Device Classification Name: Sterilizer, Chemical
Regulation Number: 880.6860
Classification Product Code: MLR
Date Received: 08/26/2009
Decision Date: 03/04/2011
Regulation Medical Specialty: General Hospital
Device Name: STERRAD 100NX STERILIZER EXPRESS CYCLE
Manufacturer: ADVANCED STERILIZATION PRODUCTS
Device Classification Name: Sterilizer, Chemical
Regulation Number: 880.6860
Classification Product Code: MLR
Date Received: 08/26/2009
Decision Date: 03/04/2011
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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