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 Enzyme Immunoassay, Cocaine And Cocaine Metabolites
510(k) Number K113501
Device Name AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP)
Applicant
Ameditech, Inc.
10340 Camino Santa Fe
San Diego,  CA  92121
Applicant Contact BRETT CASEY
Correspondent
Ameditech, Inc.
10340 Camino Santa Fe
San Diego,  CA  92121
Correspondent Contact BRETT CASEY
Regulation Number862.3250
Classification Product Code
DIO  
Subsequent Product Codes
DIS   DJC   DJG   DJR   DKZ  
JXM   JXN   LCM   LDJ   LFG  
Date Received11/25/2011
Decision Date 12/05/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Toxicology
Summary Summary
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-