Data / Medical devices / United States / Apq Health Inc
Apq Health Inc: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Apq Health Inc is registered with the FDA (registration 3042369547) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 19, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042369547
- Address
- 11845 W Olympic Blvd Ste 1100w, Los Angeles, CA, United States, 90064
- Owner or operator
- APQ Health (10094114)
- Roles
- Manufacturer
- First device listed
- November 15, 2025
- Registered through
- 2026
- Brand names listed
- Autoplaque
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| May 19, 2023 | K212758 | Autoplaque | LLZ | Substantially Equivalent | Cedars-Sinai Medical Center: Aim | accessdata.fda.gov |
Compare with other makers
Updated May 19, 2023. 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.