Cerebrotech Medical Systems Inc

FDA Filings

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

FDA Registration(s)
Registration Number3012096574
FEI Number3012096574
NameCEREBROTECH MEDICAL SYSTEMS INC
Owner & OperatorCEREBROTECH MEDICAL SYSTEMS INC
Contact Address1048 Serpentine Lane Suite 301
Pleasanton CA 94566 US
Official Correspondent
  • Dawnel Scott
  • x-510-5016571-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1048 Serpentine Ln Ste 301
Pleasanton, CA 94566 US
Establishment Type
  • Manufacture Medical Device
  • Complaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
CEREBROTECH MEDICAL SYSTEMS INC
Visor System2018-12-04
CEREBROTECH MEDICAL SYSTEMS INC
Cerebrotech Visor2018-12-04
CEREBROTECH MEDICAL SYSTEMS INC
Cerebrotech Visor2018-12-04
Cerebrotech Medical Systems, Inc.
Visor System2018-11-23
CEREBROTECH MEDICAL SYSTEMS INC
Cerebrotech Fluids Monitor 2018-03-29
CEREBROTECH MEDICAL SYSTEMS INC
Cerebrotech Fluids Monitor2015-10-19

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