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 bandage, liquid
510(k) Number K022645
Device Name CURAD
Applicant
BEIERSDORF AG
49 PLAIN ST.
NORTH ATTLEBORO,  MA  02760
Applicant Contact DANIEL J DILLON
Correspondent
BEIERSDORF AG
49 PLAIN ST.
NORTH ATTLEBORO,  MA  02760
Correspondent Contact DANIEL J DILLON
Regulation Number880.5090
Classification Product Code
KMF  
Date Received08/08/2002
Decision Date 11/05/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-