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 Biologics Clearance Letters and 510(k) Summaries Back To Search Results
Device Classification Name tubes, vials, systems, serum separators, blood collection
510(k) Number BK030001
Tradename Greiner Vacuette EDTA K3 Tube
Device Name Tubes, Vials, Systems, Serum Separators, Blood Collection
Original Applicant
Greiner Bio-One GmbH
4238 capital drive
monroe,  NC  28112
Regulation Number862.1675
Classification Product Code
JKA  
Date Received12/23/2002
Decision Date 02/26/2003
Decision substantially equivalent (SE)
Classification Advisory Committee Clinical Chemistry
Review Advisory Committee Clinical Chemistry
Type 510(k) Traditional
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product Yes
-
-