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 Drape, Surgical, Antimicrobial
510(k) Number K862577
Device Name LINEN (HUCK) TOWEL
Applicant
Dimed, Intl.
3108 Bruton Rd.
Plant City,  FL  33566
Applicant Contact CHUCK MASEK
Correspondent
Dimed, Intl.
3108 Bruton Rd.
Plant City,  FL  33566
Correspondent Contact CHUCK MASEK
Regulation Number878.4370
Classification Product Code
KKX  
Date Received07/07/1986
Decision Date 07/23/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-