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 K921760
Device Name TRICOPLAST
Applicant
BEIERSDORF, INC.
360 MARTIN LUTHER KING DR.
P.O. BOX 5529
NORWALK,  CT  06856
Applicant Contact KENNETH M NICOLL
Correspondent
BEIERSDORF, INC.
360 MARTIN LUTHER KING DR.
P.O. BOX 5529
NORWALK,  CT  06856
Correspondent Contact KENNETH M NICOLL
Regulation Number880.5240
Classification Product Code
KGX  
Date Received04/14/1992
Decision Date 08/10/1992
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
-
-