FDA.reportPublic FDA data

PROWESS, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
29392482939248PROWESS, INC.1N2026-01-015129 Commercial Circle Concord CA US 94520

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
393351369663547K984196MODIFICATION TO PROWESS PRO-SIMMUJ1998-12-11
393351058301808K231825Panther TPSMUJ2023-12-15
393351991594136K211760Panther OISIYE2021-09-28
393351723610387K193459Panther StereotacticMUJ2020-04-27
393351667212645K143514Panther StereoSeedMUJ2015-12-11
393351130693416K122616PANTHER OIS/R & V MODEL VERSION 2.0IYE2012-12-21
393351830447056K101076PROWESS PANTHER PROARC, MODEL VERSION 5.0MUJ2010-07-27
393351582747343K100801PUMA MODEL VERSION 1.0IYE2010-06-18
393351166814103K083502PANTHER REALART, MODEL 4.7MUJ2009-05-05
393351797867658K032456PROWESSMUJ2003-10-16
393351578518049
393351983509505

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MUJ122023-12-15
IYE52021-09-28

PMN#

GUDID#