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 Dressing, Wound, Drug
510(k) Number K830051
Device Name MOLNLYCKE MESALT STERILE DRESSING
Applicant
Lada Intl., Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Lada Intl., Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Classification Product Code
FRO  
Date Received01/10/1983
Decision Date 01/26/1983
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
-
-