Data / Medical devices / United States / Quintana Supply, a division of Thomas Scientific
Quintana Supply, a division of Thomas Scientific: FDA-registered device maker in Haverhill, MA, United States, 1 510(k) clearance
Quintana Supply, a division of Thomas Scientific is registered with the FDA (registration 3013418500) in Haverhill, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 27, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013418500
- Address
- 177 Ferry Rd, Haverhill, MA, United States, 01835
- Owner or operator
- QUINTANA ASSOCIATES, INC (10053852)
- Roles
- Repackager or relabeler
- First device listed
- December 7, 2020
- Registered through
- 2026
- Brand names listed
- Nasal Alar SpO2 Sensor MLT CPTL, 24/CS, Tri-anim, Nasal SpO2 Sensor, 24/CS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Oximeter | DQA | 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, 2017 | K171423 | Nasal Alar SpO2 Sensor | DQA | Substantially Equivalent | Xhale, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 27, 2017. 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.