Medical Device Manufacturer · US , Chico , CA

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

9 submissions · 9 cleared · Since 2003

Recent clearances: Panther TPS, Panther OIS, Panther Stereotactic

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.

Prowess, 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 - 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