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 System, Blood Culturing
510(k) Number K925693
Device Name EZ VIEW
Applicant
Difco Laboratories, Inc.
1180 Ellsworth Rd.
Ann Arbor,  MI  48104
Applicant Contact DAVID W GATES
Correspondent
Difco Laboratories, Inc.
1180 Ellsworth Rd.
Ann Arbor,  MI  48104
Correspondent Contact DAVID W GATES
Regulation Number866.2560
Classification Product Code
MDB  
Date Received11/12/1992
Decision Date 01/15/1993
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
-
-