• 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, Theophylline
510(k) Number K943979
Device Name IL TEST THEOPHYLLINE
Applicant
Instrumentation Laboratory CO
101 Hartwell Ave.
Lexington,  MA  02421
Applicant Contact WALLIS W CADY
Correspondent
Instrumentation Laboratory CO
101 Hartwell Ave.
Lexington,  MA  02421
Correspondent Contact WALLIS W CADY
Regulation Number862.3880
Classification Product Code
KLS  
Subsequent Product Code
DLJ  
Date Received06/07/1994
Decision Date 01/18/1995
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
-
-