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FDA 510(k), K093992, TERUMO LAUER LOCK ADAPTER
FDA 510(k), K093992, TERUMO LAUER LOCK ADAPTER
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510(K) Number: K093992
Device Name: TERUMO LAUER LOCK ADAPTER
Manufacturer: EILEEN DORSEY
Device Classification Name: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Regulation Number: DTL
Classification Product Code: 12/24/2009
Date Received: 05/19/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: TERUMO LAUER LOCK ADAPTER
Manufacturer: EILEEN DORSEY
Device Classification Name: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Regulation Number: DTL
Classification Product Code: 12/24/2009
Date Received: 05/19/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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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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