Data / Medical devices / United States / Control Medical Technology
Control Medical Technology: FDA-registered device maker in South Salt Lake, UT, United States, 4 510(k) clearances
Control Medical Technology is registered with the FDA (registration 3031788372) in South Salt Lake, UT, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated May 4, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031788372
- Address
- 2490 S 300 W, South Salt Lake, UT, United States, 84115
- Owner or operator
- Control Medical Technology (10091198)
- Roles
- Specification developer
- First device listed
- July 22, 2024
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aspiration Thrombectomy Catheter | QEZ | 2 | Specification developer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | 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 |
|---|---|---|---|---|---|---|
| May 4, 2020 | K200871 | Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator | QEZ | Substantially Equivalent | Control Medical Technology | accessdata.fda.gov |
| November 26, 2013 | K131998 | ASPIRE RX-LP6 ASPIRATION CATHETER | QEZ | Substantially Equivalent | Control Medical Technology, LLC | accessdata.fda.gov |
| February 22, 2012 | K113757 | ASPIRE MAX ASPIRATION CATHETER | QEZ | Substantially Equivalent | Control Medical Technology, LLC | accessdata.fda.gov |
| October 4, 2007 | K072299 | POWRSYRINGE ASPIRATOR | FMF | Substantially Equivalent | Pinyons Medical Technology, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 4, 2020. 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.