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FDA 510(k), K140264, MADM
FDA 510(k), K140264, MADM
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510(K) Number: K140264
Device Name: MADM
Manufacturer: CLIFF ANSEL
Device Classification Name: Gas-Machine, Anesthesia
Regulation Number: BSZ
Classification Product Code: 02/03/2014
Date Received: 01/05/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: MADM
Manufacturer: CLIFF ANSEL
Device Classification Name: Gas-Machine, Anesthesia
Regulation Number: BSZ
Classification Product Code: 02/03/2014
Date Received: 01/05/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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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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