• 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 reservoir, blood, cardiopulmonary bypass
510(k) Number K050195
Device Name V-BAG WITH GBS COATING
Applicant
GISH BIOMEDICAL, INC.
11874 SOUTH EVELYN CIRCLE
HOUSTON,  TX  77071
Applicant Contact J. HARVEY KNAUSS
Correspondent
GISH BIOMEDICAL, INC.
11874 SOUTH EVELYN CIRCLE
HOUSTON,  TX  77071
Correspondent Contact J. HARVEY KNAUSS
Regulation Number870.4400
Classification Product Code
DTN  
Date Received01/27/2005
Decision Date 03/17/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
-
-