Daxor Corp

FDA Filings

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

USAAMEXDXRDUNS 056667975
FDA Registration(s)
Registration Number3003529145
FEI Number3003857949
NameDAXOR CORPORATION
Owner & OperatorDAXOR CORPORATION
Contact Address107 Meco Lane --
Oak Ridge TN 37830 US
Official Correspondent
  • Randy - Dodgen
  • x-865-4250555-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address107 Meco Lane
Oak Ridge, TN 37830 US
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
DAXOR CORPORATION
BVA-100 Convenience Kit 9ml 2023-08-01
DAXOR CORPORATION
BVA200CONVKIT BVA200CK2023-07-20
DAXOR CORPORATION
MAX-100 2020-10-08
DAXOR CORPORATION
BVA-100 Convenience Kits 2020-10-08
DAXOR CORPORATION
BVA100 2018-10-04
DAXOR CORPORATION
MAX-100 2018-09-21
DAXOR CORPORATION
BVA100 2018-09-03
DAXOR CORPORATION
Sample Changer (SC-25)2006-06-01
DAXOR CORPORATION
BVA-100 Convenience Kit2006-06-01
DAXOR CORPORATION
Max-100 Syringe2004-02-18
DAXOR CORPORATION
BVA-100 BVA Software2004-02-18
DAXOR CORPORATION
Gamma Counter (DGX1)2004-02-18
DAXOR CORPORATION
DAXOR MAX100 SYRINGE (MAX100)1997-12-22
DAXOR CORPORATION
AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER1997-09-25

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