Data / Medical devices / United States / Hospi Corporation
Hospi Corporation: FDA-registered device maker in San Mateo, CA, United States, 1 510(k) clearance
Hospi Corporation is registered with the FDA (registration 3010761399) in San Mateo, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 24, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010761399
- Address
- 1650 S. Amphlett Blvd Suite 201, San Mateo, CA, United States, 94402
- Owner or operator
- Hospi Corporation (10046187)
- Roles
- Specification developer
- First device listed
- February 12, 2014
- Registered through
- 2026
- Brand names listed
- LiquiPill, Macy Catheter, Macy Catheter Bedside Care Kit, Macy Catheter Tray
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Enteral Administration Kit (Adult & Pediatric) | PRM | 2 | Specification developer | accessdata.fda.gov |
| Pill Crusher/Cutter | OHY | 1 | Specification developer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| January 24, 2014 | K133881 | MACY CATHETER | KNT | Substantially Equivalent | Hospi Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Pill Crusher/Cutter
- All makers of Enteral Administration Kit (Adult & Pediatric)
- All makers of Tubes, Gastrointestinal (And Accessories)
Updated January 24, 2014. 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.