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 Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K844780
Device Name EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU
Applicant
Poly- Med, Inc.
109 Industry Ln.
Cockeysville,  MD  21030
Applicant Contact FRANK S DINOTO
Correspondent
Poly- Med, Inc.
109 Industry Ln.
Cockeysville,  MD  21030
Correspondent Contact FRANK S DINOTO
Regulation Number878.4400
Classification Product Code
GEI  
Date Received12/10/1984
Decision Date 05/21/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-