Custom Interventional Pain Management

FDA Filings

This page includes the latest FDA filings for Custom Interventional Pain Management. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008552585
FEI Number3008552585
NameCUSTOM INTERVENTIONAL PAIN MANAGEMENT
Owner & OperatorCustom Interventional Pain Management
Contact Address12001 Network Blvd Ste. 208
San Antonio TX 78249 US
Official Correspondent
  • Kathleen Hann
  • x-210-8532970-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address12001 Network Blvd Ste. 208
San Antonio, TX 78249 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Discography Kit2011-11-15
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Nerve Block Tray2011-11-15
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Epidural Anesthesia Kit2011-11-15
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Custom Anesthesia Kit2011-11-15
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Spinal Anesthesia Kit2011-11-15
CUSTOM INTERVENTIONAL PAIN MANAGEMENT
Regional Anesthesia Kit2010-10-07

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