FDA.reportPublic FDA data

Precision Medical Products

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30160009733016000973Precision Medical Products1Y2026-01-013735 Cincinnati Ave Ste 100 Rocklin CA US 95765

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3025491312045669K220761CIRCUL8 Connect DVT Prevention DeviceJOW2022-06-03
3025491372496104K212731Circul8 ProJOW2021-11-15
3025491371305416K211235CIRCUL8 Luxe DVT Prevention DeviceJOW2021-09-08
3025491335090288K200285VenaOneJOW2020-07-02
3025491188744229K193020VenaPro Vascular Therapy SystemJOW2019-12-04
3025491742310525K160318PlasmaFlowJOW2016-04-01
3025491248526931
3025491412782209
3025491534952886
3025491736079117
3025491901335608
3025492032754759

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
JOW62022-06-03

PMN#

GUDID#