Data / Medical devices / Taiwan / Wu Ho Medical Instruments MFG. Co. Ltd.
Wu Ho Medical Instruments MFG. Co. Ltd.: FDA-registered device maker in Taipei Hsien, Taiwan, (China), Taiwan, 1 510(k) clearance
Wu Ho Medical Instruments MFG. Co. Ltd. is registered with the FDA (registration 8022752) in Taipei Hsien, Taiwan, (China), Taiwan. It lists 12 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 9, 1997. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 8022752
- FEI number
- 3002808508
- Address
- 5 Tzu Yu ST., Tu Cheng City, Taipei Hsien, Taiwan, (China), Taiwan, 23606
- Owner or operator
- WU HO MEDICAL INSTRU (8022752)
- Roles
- Manufacturer
- First device listed
- September 23, 1997
- Registered through
- 2027
- Brand names listed
- ARD STRETCHER, ASSEMBLY REQUIRED ANTI-TIP DEVICE, ASSEMBLY REQUIRED ARMREST, ASSEMBLY REQUIRED COMPONENT PARTS, ASSEMBLY REQUIRED CUSHION, ASSEMBLY REQUIRED FOOTREST, ASSEMBLY REQUIRED WH, INFUSION STAND and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Manufacturer | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Manufacturer | accessdata.fda.gov |
| Cushion, Wheelchair | IMP | 1 | Manufacturer | accessdata.fda.gov |
| Device, Anti-Tip, Wheelchair | IMR | 1 | Manufacturer | accessdata.fda.gov |
| Footrest, Wheelchair | IMM | 1 | Manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Manufacturer | accessdata.fda.gov |
| Stool, Operating-Room | FZM | 1 | Manufacturer | accessdata.fda.gov |
| Stretcher, Wheeled | FPO | 2 | Manufacturer | accessdata.fda.gov |
| Tips And Pads, Cane, Crutch And Walker | INP | 1 | Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 9, 1997 | K973418 | UNIVERSAL/1000 SERIES(101S101SDU1100)/ROLLS 2000(2000E)/TRANSPORT(M4) | IOR | Substantially Equivalent | Assembly Required Dist., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stool, Operating-Room
- All makers of Device, Anti-Tip, Wheelchair
- All makers of Footrest, Wheelchair
- All makers of Stand, Infusion
- All makers of Components, Wheelchair
- All makers of Armrest, Wheelchair
Updated October 9, 1997. 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.