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 Linked Immunoabsorbent Assay, Toxoplasma Gondii
510(k) Number K903968
Device Name TOXO-CUBE
Applicant
Difco Laboratories, Inc.
1180 Ellsworth Rd.
Ann Arbor,  MI  48104
Applicant Contact WALTER FISCHER
Correspondent
Difco Laboratories, Inc.
1180 Ellsworth Rd.
Ann Arbor,  MI  48104
Correspondent Contact WALTER FISCHER
Regulation Number866.3780
Classification Product Code
LGD  
Date Received08/28/1990
Decision Date 12/18/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-