Greiner Bio-One Na, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Greiner Bio-One Na, Inc. has 5 FDA 510(k) cleared medical devices. Based in Monroe, US.
Historical record: 5 cleared submissions from 2016 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Greiner Bio-One Na, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Greiner Bio-One Na, Inc.
5 devices
Cleared
Jan 25, 2019
MiniCollect K2E K2EDTA Tubes
Hematology
176d
Cleared
May 21, 2018
VACUETTE SAFELINK Holder with male luer lock
General Hospital
81d
Cleared
Apr 19, 2018
VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set
General Hospital
129d
Cleared
Mar 06, 2017
Greiner Vacuette Urine Count and Culture, Mannitol tube
Microbiology
89d
Cleared
Nov 03, 2016
Greiner Holdex
General Hospital
251d