Peter Schiff Enterprise

FDA Filings

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

FDA Registration(s)
Registration Number1044143
FEI Number1000112898
NamePETER SCHIFF ENTERPRISE
Owner & OperatorPETER SCHIFF ENTERPRISE
Contact Address4900 FORREST HILL RD. --
Cookeville TN 38506 US
Official Correspondent
  • Janice Scarlett
  • x-931-5376505-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4900 Forrest Hill Rd
COOKEVILLE, TN 38506 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
PETER SCHIFF ENTERPRISE
Peter Schiff AC Fibrillator Model #310C2010-03-09
PETER SCHIFF ENTERPRISE
VARIOUS SIZES OF ELECTRODE CABLES2002-04-16

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.