Ischemaview Inc

FDA Filings

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

FDA Registration(s)
Registration Number3011205675
FEI Number3011205675
NameISCHEMAVIEW, INC.
Owner & OperatoriSchemaView, Inc.
Contact Address433 Park Point Drive Suite 220
Golden CO 80401 US
Official Correspondent
  • James R Rosa
  • 001-303-7043374-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address433 Park Point Drive Suite 220
Golden, CO 80401 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
ISchemaView Inc.
Rapid ASPECTS2020-06-26
ISCHEMAVIEW, INC.
Rapid 2020-05-14
ISCHEMAVIEW, INC.
RAPID Rapid2020-04-15
ISCHEMAVIEW, INC.
RAPID 2020-04-15
ISCHEMAVIEW, INC.
RAPID 2020-04-15
ISCHEMAVIEW, INC.
RAPID Rapid2020-04-15
ISCHEMAVIEW, INC.
RAPID Rapid2020-04-15
ISchemaView Incorporated
Rapid ICH2020-03-31
ISCHEMAVIEW, INC.
RAPID RAPID2019-06-20
ISCHEMAVIEW, INC.
RAPID2019-06-10
ISchemaView, Inc.
ISchemaView RAPID2018-12-27
ISCHEMAVIEW, INC.
RAPID2018-08-20
ISchemaView, Inc.
ISchemaView RAPID2018-04-19
ISCHEMAVIEW, INC.
RAPID2014-10-24

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