• 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 Dressing, Wound And Burn, Occlusive
510(k) Number K951842
Device Name BIODERM MEDICAL TRANSPARENT FILM DRESSING
Applicant
Bioderm, Inc.
P.O. Box 4882
Wheaton,  IL  60189
Applicant Contact GEORGE WORTHLEY
Correspondent
Bioderm, Inc.
P.O. Box 4882
Wheaton,  IL  60189
Correspondent Contact GEORGE WORTHLEY
Classification Product Code
MGP  
Date Received04/20/1995
Decision Date 06/12/1995
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-