• 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 K925660
Device Name KTI TRANSPARENT WOUND DRESSING
Applicant
Kingston Technologies, Inc.
2235 Rte. 130
Dayton,  NJ  08810
Applicant Contact KEN BLASHKA
Correspondent
Kingston Technologies, Inc.
2235 Rte. 130
Dayton,  NJ  08810
Correspondent Contact KEN BLASHKA
Classification Product Code
MGP  
Date Received11/10/1992
Decision Date 04/20/1993
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
-
-