Astek Technology L T D

FDA Filings

This page includes the latest FDA filings for Astek Technology L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013077196
FEI Number3013077196
NameKristine Van Der Hoeven
Owner & OperatorASTEK Technology Ltd.
Contact AddressNo.118, Taizih Rd. Rende Hsiang, Tainan
Tainan TW-TNQ Tainan - District 717 TW
Official Correspondent
  • You-Jhe Lin
  • 886-6-2729488-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5039 88th Avenue SE
Mercer Island, WA 98040 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-502020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-252020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-202020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS Stimulator AK-10M2020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-502020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-252020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS and EMS Stimulator AK3-202020-02-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
TENS Stimulator AK-10M2020-02-11
Astek Technology Ltd.
TENS And EMS Stimulator, TENS Stimulator2020-01-11
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
EPG050050;EPG053083;EPL050050;EPL073150;EPP050050;EPP118058;EPP0480002019-10-07
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
AK360;AK368;AK370;AK660;AK770;AK880;AK10MA;AK325A;AK320A;AK350A;AK500;AK510;AK520;KR1300;KR1600;AK100;2019-10-07
Kristine Van Der Hoeven [ASTEK Technology Ltd.]
AK100B;AK100C;AK100D;AK101;AK101B;AK101C;AK101D;AK350AIFT;EPB047047;EPB047098;EPD090147;EPD105203;EPG046046;2019-10-07

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