FDA 510(k) Applications Submitted by GREINER MEDITECH, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K991843 |
05/28/1999 |
GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE |
GREINER MEDITECH, INC. |
K992244 |
07/02/1999 |
GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE |
GREINER MEDITECH, INC. |
K982998 |
08/27/1998 |
GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE |
GREINER MEDITECH, INC. |
K982999 |
08/27/1998 |
GREINER MINICOLLECT EDTA BLOOD COLLECTION TUBE |
GREINER MEDITECH, INC. |
K983952 |
11/05/1998 |
GREINER VACUETTE BLOOD COLLECTION TUBE |
GREINER MEDITECH, INC. |
K980768 |
02/27/1998 |
VACUETTE HOLDEX |
GREINER MEDITECH, INC. |
K981619 |
05/06/1998 |
VACUETTE MULTIPLE SAMPLE LUER ADAPTER |
GREINER MEDITECH, INC. |
K992145 |
06/24/1999 |
ECOMED SCALP VEIN SET |
GREINER MEDITECH, INC. |
K973620 |
09/23/1997 |
VACUETTE MULTI-SAMPLE NEEDLE |
GREINER MEDITECH, INC. |
K974873 |
12/29/1997 |
VACUETTE (MULTI-USE HOLDER) |
GREINER MEDITECH, INC. |
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