Medical Device Manufacturer · US , Chico , CA

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

9 submissions · 9 cleared · Since 2003

9

Total

9

Cleared

0

Denied

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

Last cleared in 2023. Active since 2003. Primary specialty: Radiology.

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

FDA 510(k) cleared devices by Prowess, Inc.

9 devices

1-9 of 9

Cleared Dec 15, 2023

Radiology · 177d

Cleared Sep 28, 2021

Radiology · 112d

Cleared Apr 27, 2020

Panther Stereotactic

Radiology · 133d

Cleared Dec 11, 2015

Panther StereoSeed

Radiology · 365d

Cleared Dec 21, 2012

PANTHER OIS/R & V MODEL VERSION 2.0

Radiology · 116d

Cleared Jul 27, 2010

PROWESS PANTHER PROARC, MODEL VERSION 5.0

Radiology · 99d

Cleared Jun 18, 2010

PUMA MODEL VERSION 1.0

Radiology · 88d

Cleared May 05, 2009

PANTHER REALART, MODEL 4.7

Radiology · 161d

Cleared Oct 16, 2003

Radiology · 66d