Perimed Inc

FDA Filings

This page includes the latest FDA filings for Perimed Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Perimed Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number2246823
FEI Number2246823
NamePERIMED INC
Owner & OperatorPerimed Inc
Contact Address7485 W Azure Drive, Suite 126
Las Vegas NV 89130 US
Official Correspondent
  • Samuel Pakvis
  • x-702-9874655-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address7485 W Azure Drive, Suite 126
Las Vegas, NV 89130 US



FDA Filings

Device
Company
DeviceDate
PERIMED, INC.
PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)1999-09-23
PERIMED, INC.
PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT1998-05-28
PERIMED, INC.
PF404/409/410/411/416/418 W/PF319:0/319:1/319:21994-04-18
PERIMED, INC.
PERITEMP PF 4005 HEATER1993-12-07
PERIMED, INC.
PERIFLUX PF4001 LASER DOPPLER FLOWMETER1993-02-03
PERIMED, INC.
PERIFLUX PF31989-06-20

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.