FDA.reportPublic FDA data

DSRV, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30047375293004737529DSRV, INC.1N2026-01-01330 Waterloo Valley Rd Suite 200 Mount Olive NJ US 07828

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
768571334030563K993332GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05GGC2000-02-16
768571485572623K922326LUPO-TEST REGEANTGIR1993-04-06
768572010494917K922156LUCOR CONFIRMATORY REAGENTGIR1993-04-06
768571049226879K132130REAGENT, RUSSEL VIPER VENOM - LA SCREENGIR2014-01-10
768571255323607K132076REAGENT, RUSSEL VIPER VENOM - LA CONFIRMGIR2014-01-10
768571043070131
768571054991639
768571086966027
768571303184576

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GIR42014-01-10
GGC12000-02-16

PMN#

GUDID#