Medical Device Manufacturer · US , Bel Air , MD

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

10 submissions · 10 cleared · Since 1997

Total

Cleared

Denied

Greiner Meditech, Inc. has 10 FDA 510(k) cleared medical devices. Based in Bel Air, US.

Historical record: 10 cleared submissions from 1997 to 1999. Primary specialty: Chemistry.

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

Greiner Meditech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

10 devices

1-10 of 10

Cleared Oct 14, 1999

ECOMED SCALP VEIN SET

K992145 · FPA

General Hospital · 112d

Cleared Jul 26, 1999

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE

K992244 · JKA

Chemistry · 24d

Cleared Jun 25, 1999

GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE

K991843 · JKA

Chemistry · 28d

Cleared Dec 28, 1998

GREINER VACUETTE BLOOD COLLECTION TUBE

K983952 · JKA

Chemistry · 53d

Cleared Oct 21, 1998

GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE

K982998 · JKA

Chemistry · 55d

Cleared Oct 16, 1998

GREINER MINICOLLECT EDTA BLOOD COLLECTION TUBE

K982999 · JKA

Chemistry · 50d

Cleared Jul 15, 1998

VACUETTE MULTIPLE SAMPLE LUER ADAPTER

K981619 · FMI

General Hospital · 70d

Cleared Apr 09, 1998

VACUETTE HOLDEX

K980768 · FMI

General Hospital · 41d

Cleared Feb 05, 1998

VACUETTE (MULTI-USE HOLDER)

K974873 · JKA

Chemistry · 38d

Cleared Dec 17, 1997

VACUETTE MULTI-SAMPLE NEEDLE

K973620 · FMI

General Hospital · 85d

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

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

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