Medical Device Manufacturer · US , Wilmington , DE

Greiner America, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1996

Recent clearances: GREINER VACUETTE BLOOD COLLECTION TUBE, GREINER VACUETTE BLOOD COLLECTION TUBE, GREINER VACUETTE BLOOD COLLECTION TUBE

7

Total

7

Cleared

0

Denied

Greiner America, Inc. has 7 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Historical record: 7 cleared submissions from 1996 to 1997. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Greiner America, Inc. Filter by specialty or product code using the sidebar.

Greiner America, Inc. is one of 7844 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Greiner America, Inc.

7 devices

1-7 of 7

Cleared Jun 04, 1997

GREINER VACUETTE BLOOD COLLECTION TUBE

Chemistry · 63d

Cleared May 12, 1997

GREINER VACUETTE BLOOD COLLECTION TUBE

Toxicology · 40d

Cleared May 12, 1997

GREINER VACUETTE BLOOD COLLECTION TUBE

Chemistry · 40d

Cleared May 02, 1997

GREINER VACUETTE BLOOD COLLECTION TUBE

Chemistry · 30d

Cleared Sep 05, 1996

GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3

Chemistry · 188d

Cleared Aug 30, 1996

GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR

Chemistry · 182d

Cleared Aug 30, 1996

GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR

Chemistry · 182d