Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 Tape And Bandage, Adhesive
510(k) Number K896733
Device Name VACCON
Applicant
UNOPLAST A/S
DK-3390 HUNDESTED
DENMARK,  DK
Applicant Contact ERIK ANDERSEN
Correspondent
UNOPLAST A/S
DK-3390 HUNDESTED
DENMARK,  DK
Correspondent Contact ERIK ANDERSEN
Regulation Number880.5240
Classification Product Code
KGX  
Date Received11/30/1989
Decision Date 02/01/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-