• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name shunt, central nervous system and components
510(k) Number K172759
Device Name Smart External Drain (SED) System
Applicant
Aqueduct Critical Care, Inc.
11822 North Creek Parkway North
Suite 110
Bothell,  WA  98011
Applicant Contact Thomas Clement
Correspondent
Aqueduct Critical Care, Inc.
11822 North Creek Parkway North
Suite 110
Bothell,  WA  98011
Correspondent Contact Thomas Clement
Regulation Number882.5550
Classification Product Code
JXG  
Subsequent Product Code
GWM  
Date Received09/13/2017
Decision Date 11/14/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-