Data / Medical devices / Infant Pulse Rate And Oxygen Saturation Monitor For Over-The-Counter Use
Infant Pulse Rate And Oxygen Saturation Monitor For Over-The-Counter Use (QYU): 4 FDA-registered makers in 3 countries
4 establishments in 3 countries are registered with the FDA to make Infant Pulse Rate And Oxygen Saturation Monitor For Over-The-Counter Use (product code QYU, Class 2, 21 CFR 870.2705). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on May 3, 2024, and lists 0 recall events (0 Class I). FDA data exported November 3, 2026.
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- Product code
- QYU
- Device class
- 2
- Regulation
- 870.2705
- Medical specialty
- Cardiovascular
Makers by country
| Country | Makers |
|---|---|
| United States | 2 |
| Mexico | 1 |
| Thailand | 1 |
Makers of Infant Pulse Rate And Oxygen Saturation Monitor For Over-The-Counter Use
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Industrial Vallera de Mexicali, S. A. de C. V. | Mexicali Mexico, Mexico | Manufacturer | 1 | May 3, 2024 | 0 | 0 | 0 | api.fda.gov |
| Masimo Corporation | Irvine, CA, United States | Complaint file establishment, Specification developer | 1 | May 3, 2024 | 0 | 0 | 0 | api.fda.gov |
| Owlet Baby Care | Lehi, UT, United States | Complaint file establishment, Specification developer | 1 | November 8, 2023 | 0 | 0 | 0 | api.fda.gov |
| Benchmark Electronics (thailand) Public Company Li | AYUDHAYA Phra Nakhon Si Ayutthaya, Thailand | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 3, 2024. 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.