• 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 Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
510(k) Number K791797
Device Name MTS CATHETER ADAPTER FOR GUIDANCE ENTRY
Applicant
Medical Testing System, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medical Testing System, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4290
Classification Product Code
DTL  
Date Received09/14/1979
Decision Date 10/11/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-