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 U.V. Spectrometry, Theophylline
510(k) Number K780442
Device Name THEOPHYLLINE ASSAY TO THE GEMSAEC
Applicant
Syva Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Syva Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.3880
Classification Product Code
LCY  
Date Received03/20/1978
Decision Date 04/12/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-