Data / Medical devices / United States / Protocol Solutions LLC
Protocol Solutions LLC: FDA-registered device maker in Branson, MO, United States, 1 510(k) clearance
Protocol Solutions LLC is registered with the FDA (registration 3030338883) in Branson, MO, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 8, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030338883
- Address
- 225 Violyn Dr, Branson, MO, United States, 65616
- Owner or operator
- Protocol Solutions LLC (10089852)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- January 15, 2024
- Registered through
- 2026
- Brand names listed
- NERVE CARE+
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Complaint file establishment | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| April 8, 2004 | K040253 | EASY MED TN-28 C | GZJ | Substantially Equivalent | Easy Med Instrument Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Vibrator, Therapeutic
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
Updated April 8, 2004. 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.