Intermetro De Acuna

FDA Filings

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

FDA Registration(s)
Registration Number3009526986
FEI Number3009526986
NameInterMetro de Acuna
Owner & OperatorINTERMETRO INDUSTRIES CORP.
Contact Address651 NORTH WASHINGTON ST. --
Wilkes Barre PA 18705 US
Official Correspondent
  • Willard J Sickles
  • x-570-7063121-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressCalle Zacatecas 505 Parque Industrial Amistad
Acuna Coahuila, 26220 MX
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
InterMetro de Acuna [INTERMETRO INDUSTRIES CORP.]
Lifeline Code Response2005-05-03
InterMetro de Acuna [INTERMETRO INDUSTRIES CORP.]
Flexline Code Response2005-05-03
InterMetro de Acuna [INTERMETRO INDUSTRIES CORP.]
Starsys Anesthesia Cart1996-09-09
InterMetro de Acuna [INTERMETRO INDUSTRIES CORP.]
Flexline Anesthesia1996-09-09

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