Data / Medical devices / United States / Parvo Medics Inc.
Parvo Medics Inc.: FDA-registered device maker in Murray, UT, United States, 1 510(k) clearance
Parvo Medics Inc. is registered with the FDA (registration 1725061) in Murray, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 16, 1995. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1725061
- FEI number
- 3003009503
- Address
- 6526 S State St Ste 202, Murray, UT, United States, 84107
- Owner or operator
- ParvoMedics, Inc. (10061327)
- Roles
- Manufacturer
- First device listed
- October 8, 2019
- Registered through
- 2027
- Brand names listed
- TrueOne 2400
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Calculator, Pulmonary Function Data | BZC | 2 | 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 |
|---|---|---|---|---|---|---|
| June 16, 1995 | K941843 | MMS-2400 | BZC | Substantially Equivalent | Parvo Medics, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 16, 1995. 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.