Medical Device Manufacturer · US , Atlanta , GA

Syntermed, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2000

Total

Cleared

Denied

Syntermed, Inc. has 12 FDA 510(k) cleared radiology devices. Based in Atlanta, US.

Historical record: 12 cleared submissions from 2000 to 2013.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Syntermed, 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 - Syntermed, Inc.

12 devices

1-12 of 12

Cleared Jun 14, 2013

EMORY CARDIAC TOOLBOX 3.2

EMORY CARDIAC TOOLBOX 4.0

K123646 · KPS

Radiology · 87d

Cleared Mar 14, 2008

QUANTITATIVE NEUROQ 3.0

K072307 · KPS

Radiology · 210d

Cleared Jul 26, 2007

SYSTEM, TOMOGRAPHY, COMPUTED EMISSION

EMORY CARDIAC TOOLBOX VERSION 2.6

K040141 · KPS

Radiology · 8d

Cleared Apr 23, 2002

NORTHWESTERN GATED BLOOD POOL SPECT (NUMUGAS)

K020300 · KPS

Radiology · 84d

Cleared Feb 22, 2002

EMORY CARDIAC TOOLBOX 2.1 EXECUTING ON NUCLEAR MEDICINE COMPUTERS

K014033 · KPS

Radiology · 77d

Cleared Jul 17, 2000

MEDICAL IMAGE MERGE (MIM)

K001276 · KPS

Radiology · 87d

Syntermed, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Syntermed, Inc.

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