Medical Device Manufacturer · US , Telford , PA

Drager Medizintechnik GmbH - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1999

8

Total

8

Cleared

0

Denied

Drager Medizintechnik GmbH has 8 FDA 510(k) cleared medical devices. Based in Telford, US.

Historical record: 8 cleared submissions from 1999 to 2003. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Drager Medizintechnik GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Drager Medizintechnik GmbH

8 devices

1-8 of 8

Cleared Jan 15, 2003

OPTION NIV, MODEL 8414115, UPGRADE KIT NIV, MODEL 8414072

Anesthesiology · 105d

Cleared Dec 20, 2001

OXYLOG 1000, MODEL 2M86840

Anesthesiology · 279d

Cleared Sep 04, 2001

VENTVIEW, MODEL 8414095

Anesthesiology · 54d

Cleared Jun 25, 2001

Anesthesiology · 266d

Cleared Jun 14, 2001

NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474

Anesthesiology · 154d

Cleared Jun 07, 2001

SOLA 700,SOLA 500, SOLA 300

General & Plastic Surgery · 87d

Cleared Dec 13, 2000

General Hospital · 72d

Cleared Mar 29, 1999

DRAGER SOLA SERIES, MODELS 1000/700/500/300

General & Plastic Surgery · 90d