Medical Device Manufacturer · US , Kirkland , WA

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

9 submissions · 9 cleared · Since 2002

Total

Cleared

Denied

Confirma, Inc. has 9 FDA 510(k) cleared medical devices. Based in Kirkland, US.

Historical record: 9 cleared submissions from 2002 to 2009. Primary specialty: Radiology.

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

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

9 devices

1-9 of 9

CADSTREAM, VERSION 5.0

K081556 · LLZ

Radiology · 244d

Cleared Jul 09, 2007

CONFIRMA BREAST MRI INTERVENTIONAL COMPONENTS

K071534 · MOS

Radiology · 34d

Cleared Mar 29, 2006

ACCESS BREAST COIL 4/SMS

CADSTREAM VERSION 4.0

K043216 · LLZ

Radiology · 45d

Cleared Jul 07, 2004

CADSTREAM VERSION 3.1

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

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