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FDA 510(k), K060618, CIDEX ACTIVATED DIALDEHYDE SOLUTION
FDA 510(k), K060618, CIDEX ACTIVATED DIALDEHYDE SOLUTION
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510(K) Number: K060618
Device Name: CIDEX ACTIVATED DIALDEHYDE SOLUTION
Manufacturer: JOHNSON & JOHNSON CO.
Device Classification Name: sterilant, medical devices
Regulation Number: 880.6885
Classification Product Code: MED
Date Received: 03/08/2006
Decision Date: 04/12/2006
Regulation Medical Specialty: General Hospital
Device Name: CIDEX ACTIVATED DIALDEHYDE SOLUTION
Manufacturer: JOHNSON & JOHNSON CO.
Device Classification Name: sterilant, medical devices
Regulation Number: 880.6885
Classification Product Code: MED
Date Received: 03/08/2006
Decision Date: 04/12/2006
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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