Cuattro L L C

FDA Filings

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

FDA Registration(s)
Registration Number3008364043
FEI Number3008364043
NameCUATTRO LLC
Owner & OperatorCuattro LLC
Contact Address150 Capital Drive Suite 280
Golden CO 80401 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address150 Capital Drive Suite 280
Golden, CO 80401 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
CUATTRO LLC
Cuattro ONE Long Format Digital Radiography2019-07-08
CUATTRO LLC
CuattroDR2017-05-17
CUATTRO LLC
CuattroDR2017-05-17
Cuattro, LLC
CuattroDR2016-10-06
CUATTRO LLC
Arcus2011-12-09
CUATTRO LLC
Cuattro CloudDR2010-04-07
CUATTRO, LLC
CUATTRO UNOMD2010-03-05

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