Shelly Ast

FDA Filings

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

FDA Registration(s)
Registration Number9611481
FEI Number3002807220
NameShelly Ast
Owner & OperatorHAKKO CO., LTD.
Contact AddressNO. 3055 O-AZA TOGURAONSEN CHIKUMA-SHI
NAGANO JP-NOTA 389-0807 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3726 Lonsdale St.
Cincinnati, OH 45227 US
Establishment Type
  • Manufacture Medical Device
  • Sterilize Medical Device for Another Party (Contract Sterilizer)



FDA Filings

Device
Company
DeviceDate
Shelly Ast [HAKKO CO., LTD.]
Stimuplex (DIG,RC, A)2012-12-14
Shelly Ast [HAKKO CO., LTD.]
Echostim Facet Tip2012-02-10
Shelly Ast [HAKKO CO., LTD.]
Tuohy Epidural Needle2007-11-13
Shelly Ast [HAKKO CO., LTD.]
Hakko Spinal Needle2007-11-13
Shelly Ast [HAKKO CO., LTD.]
Sonopsy Needle2007-11-13
Shelly Ast [HAKKO CO., LTD.]
Biosuc Fine Aspiration2007-11-13
Shelly Ast [HAKKO CO., LTD.]
ACCUTARG2001-11-13

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