Yurtcraft

FDA Filings

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

FDA Registration(s)
Registration Number3011299952
FEI Number3011299952
NameYURTCRAFT
Owner & OperatorYURTCRAFT
Contact Address2703 Byrne Pl
Wichita Falls TX 76306 US
Official Correspondent
  • Lisa Allbee
  • 1-940-2358310-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2703 Byrne Pl
Wichita Falls, TX 76306 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
YURTCRAFT
yurtcraft pads2014-12-15

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