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 Alcohol Control Materials
510(k) Number K935819
Device Name QUALITY CONTROL MATERIAL (ASSAYED)
Applicant
Columbia Diagnostics, Inc.
8001 Research Way
Springfield,  VA  22153
Applicant Contact STANLEY P GOLDENBERG
Correspondent
Columbia Diagnostics, Inc.
8001 Research Way
Springfield,  VA  22153
Correspondent Contact STANLEY P GOLDENBERG
Regulation Number862.3280
Classification Product Code
DKC  
Date Received12/03/1993
Decision Date 03/22/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-