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FDA 510(k), K123546, 3M ATTEST(TM) AUTO-READER
FDA 510(k), K123546, 3M ATTEST(TM) AUTO-READER
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510(K) Number: K123546
Device Name: 3M ATTEST(TM) AUTO-READER
Manufacturer: 3M COMPANY
Device Classification Name: indicator, biological sterilization process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 11/19/2012
Decision Date: 03/18/2013
Regulation Medical Specialty: General Hospital
Device Name: 3M ATTEST(TM) AUTO-READER
Manufacturer: 3M COMPANY
Device Classification Name: indicator, biological sterilization process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 11/19/2012
Decision Date: 03/18/2013
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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