• 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 Catheter And Tip, Suction
510(k) Number K871950
Device Name VIA-GUARD
Applicant
Surgimark, Inc.
4706 W. Nob Hill Blvd.
Yakima,  WA  98908
Applicant Contact RICHARD J YARGER,MD
Correspondent
Surgimark, Inc.
4706 W. Nob Hill Blvd.
Yakima,  WA  98908
Correspondent Contact RICHARD J YARGER,MD
Regulation Number880.6740
Classification Product Code
JOL  
Date Received05/20/1987
Decision Date 07/23/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-