Aerscher Diagnostics

FDA Filings

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

FDA Registration(s)
Registration Number1123776
FEI Number1000219815
NameAERSCHER DIAGNOSTICS
Owner & OperatorAERSCHER DIAGNOSTICS
Contact Address125 Dixon Drive --
Chestertown MD 21620 US
Official Correspondent
  • ROBERT - SCHREIBER
  • x-410-7781144-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address125 Dixon Drive
CHESTERTOWN, MD 21620 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
AERSCHER DIAGNOSTICS
HemaPrompt2008-01-02
AERSCHER DIAGNOSTICS
HemaPrompt2008-01-02
AERSCHER DIAGNOSTICS
HEMAPROMPT GASTRIC2003-09-24
AERSCHER DIAGNOSTICS
HEMAPROMPT1998-09-15
AERSCHER DIAGNOSTICS
HEMAPROMPT1997-10-20

Related Finance Registrations
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.