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 Snake Bite Suction Kit
510(k) Number K844048
Device Name DR. HESSEL'S INSECT POISON REMOVER
Applicant
Medie Group
1819 He St. NW
Federal Bar Bldg.
Washington,  DC  20006
Applicant Contact RANDI L BRESLOW
Correspondent
Medie Group
1819 He St. NW
Federal Bar Bldg.
Washington,  DC  20006
Correspondent Contact RANDI L BRESLOW
Regulation Number880.5740
Classification Product Code
KYP  
Date Received10/17/1984
Decision Date 01/23/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-