Data / Medical devices / United States / Future Health Concepts, Inc.
Future Health Concepts, Inc.: FDA-registered device maker in Sanford, FL, United States, 1 510(k) clearance
Future Health Concepts, Inc. is registered with the FDA (registration 1033902) in Sanford, FL, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 5, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1033902
- Address
- 1211 E. 30th Street, Sanford, FL, United States, 32773
- Owner or operator
- Future Health Concepts, Inc. (10062131)
- Roles
- Repackager or relabeler
- First device listed
- December 20, 2019
- Registered through
- 2026
- Brand names listed
- FACC0130, FACC2200, FHC1000, FHC7100, FHC7100-EYE1, FHCDWC24, FHCDWC24-G, FHCDWC2424 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stretcher, Hand-Carried | FPP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stretcher, Wheeled | FPO | 2 | Repackager or relabeler | accessdata.fda.gov |
| Table, Operating-Room, Ac-Powered | FQO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Warmer, Thermal, Infusion Fluid | LGZ | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| March 5, 2019 | K180842 | MAC Medical D-Series Blanket and Solution Warming Cabinets | LGZ | Substantially Equivalent | Mac Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Table, Operating-Room, Ac-Powered
- All makers of Warmer, Thermal, Infusion Fluid
- All makers of Stretcher, Wheeled
- All makers of Stretcher, Hand-Carried
Updated March 5, 2019. 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.