FDA.reportPublic FDA data

Ankur Kaushal

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30435344833043534483Ankur Kaushal1N2026-01-01150 Baytech Dr San Jose CA US 95134

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3481361555933137K251082HYDROS Robotic System (HY1000); HYDROS Handpiece (HH1000); HYDROS TRUS Probe (HU1000)PZP2025-10-10
3481361606498837K240200HYDROS Robotic System; HYDROS TRUS Probe; HYDROS HandpiecePZP2024-08-20
3481361128611049K173000Apogee 2100 Digital Color Doppler Ultrasound Imaging System Apogee 2300 Digital Color Doppler Ultrasound Imaging SystemIYN2017-12-07
3481361623310986

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PZP22025-10-10
IYN12017-12-07