Data / Medical devices / Taiwan / Home Care Technology Co., Ltd.
Home Care Technology Co., Ltd.: FDA-registered device maker in Tainan City, Taiwan, 5 510(k) clearances
Home Care Technology Co., Ltd. is registered with the FDA (registration 9710580) in Tainan City, Taiwan. It lists 7 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 29, 2003. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9710580
- FEI number
- 3003514353
- Address
- 116, Lane 523, Sec.3, Jung Jeng RD., Jen Ter District, Tainan City, Taiwan, 71757
- Owner or operator
- HOME CARE TECHNOLOGY CO., LTD. (9044639)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- February 5, 2001
- Registered through
- 2027
- Brand names listed
- Electrode Wire and Cable, HOME CARE, HOME CARE COLD, HOME CARE HT701 SERIES, HOT PACK, HT-326L, HT-329M Series, Home Care and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable, Electrode | IKD | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Electrode, Cutaneous | GXY | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Media, Electroconductive | GYB | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 29, 2003 | K023000 | HOME CARE VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-329M SERIES | IPF | Substantially Equivalent | Home Care Technology Co., Ltd. | accessdata.fda.gov |
| May 20, 2003 | K022998 | HOME CARE VAREIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-311, HT-311N, HT-312 | IPF | Substantially Equivalent | Home Care Technology Co., Ltd. | accessdata.fda.gov |
| April 8, 2003 | K023001 | HOME CARE VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-326L | IPF | Substantially Equivalent | Home Care Technology Co., Ltd. | accessdata.fda.gov |
| March 4, 2003 | K022917 | HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES | GXY | Substantially Equivalent | Home Care Technology Co., Ltd. | accessdata.fda.gov |
| December 2, 2002 | K022494 | HOME CARE JELLY | GYB | Substantially Equivalent | Roc Chinese-European Industrial Research Society | accessdata.fda.gov |
Compare with other makers
- All makers of Cable, Electrode
- All makers of Stimulator, Muscle, Powered
- All makers of Massager, Therapeutic, Electric
- All makers of Electrode, Cutaneous
- All makers of Media, Electroconductive
- All makers of Pack, Hot Or Cold, Reusable
Updated October 29, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.