Data / Medical devices / United States / Innovative Patient Support Solutions, LLC
Innovative Patient Support Solutions, LLC: FDA-registered device maker in Cazenovia, NY, United States, 1 510(k) clearance
Innovative Patient Support Solutions, LLC is registered with the FDA (registration 3016075711) in Cazenovia, NY, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 27, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016075711
- Address
- 5345 Indian Lookout Rd., Cazenovia, NY, United States, 13035
- Owner or operator
- Innovative Patient Support Solutions, LLC (10062768)
- Roles
- Repackager or relabeler
- First device listed
- March 6, 2020
- Registered through
- 2026
- Brand names listed
- NCODA Treatment Support Kit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Hot/Cold Water | FPF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Repackager or relabeler | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 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 |
|---|---|---|---|---|---|---|
| July 27, 2005 | K050463 | CLEVER TD-1107 EAR/SKIN/SURFACE IR THERMOMETER, CLEVER TD-1110 EAR/SKIN/SURFACE IR THERMOMETER | FLL | Substantially Equivalent | Taidoc Technology Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Bottle, Hot/Cold Water
- All makers of Pack, Hot Or Cold, Reusable
- All makers of Dispenser, Solid Medication
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
Updated July 27, 2005. 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.