FDA.reportPublic FDA data

PROACT, LTD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
21838392183839PROACT, LTD.1N2020-04-252452 General Potter Hwy. Centre Hall PA US 16828

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
360001652225472K941256QUICK CORE IIKNW1994-07-13
360001771314744K926559PROACT BIOPSY NEEDLE ENCHANCEMENTSFCG1993-03-22
360001444178226K902320BAUER FLEXI-TEMNO BIOPSY NEEDLEFCG1990-10-01
360001735242919K902319BAUER TEMNO BIOPSY NEEDLEFCG1990-09-06
360001311413265K843816TAL-CLIPGDJ1984-10-31

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FCG31993-03-22
KNW11994-07-13
GDJ11984-10-31

PMN#