Medical Device Manufacturer · US , Ellicott City , MD

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

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Greiner Vacuette North America, Inc. has 5 FDA 510(k) cleared medical devices. Based in Ellicott City, US.

Historical record: 5 cleared submissions from 2000 to 2002. Primary specialty: Chemistry.

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

Greiner Vacuette North America, 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 Vacuette North America, Inc.

5 devices

1-5 of 5