Data / Medical devices / United States / Cables And Sensors, LLC
Cables And Sensors, LLC: FDA-registered device maker in Orlando, FL, United States, 5 510(k) clearances
Cables And Sensors, LLC is registered with the FDA (registration 3008595074) in Orlando, FL, United States. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated June 8, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008595074
- Address
- 5874 S Semoran BLVD, Orlando, FL, United States, 32822
- Owner or operator
- Cables and Sensors, LLC (10039590)
- Roles
- Complaint file establishment
- First device listed
- October 11, 2021
- Registered through
- 2026
- Brand names listed
- Cables and Sensors, Oximetry sensors, SpO2 sensors, pulse oximeter cable
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Oximeter | DQA | 2 | Complaint file establishment | 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 8, 2018 | K172981 | Reusable SpO2 Sensors, Disposable SpO2 Sensors | DQA | Substantially Equivalent | APK Technology Co., Ltd. | accessdata.fda.gov |
| February 6, 2015 | K142832 | Unimed Disposable and Reusable SPO2 Sensors | DQA | Substantially Equivalent | Unimed Medical Supplies, Inc. | accessdata.fda.gov |
| August 20, 2009 | K083448 | CABLE, TRANSDUCER, MODEL 2400GN | DQA | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| April 3, 2009 | K082846 | APK SPO2 PULSE OXIMETER SENSOR | DQA | Substantially Equivalent | APK Technology Co., Ltd. | accessdata.fda.gov |
| December 2, 2008 | K082546 | REUSABLE OHMEDA (U410-02), DATEX (U410-09) COMPATABLE ADULT FINGER CLIP SENSOR, PHILLIPS ADULT SOFT TIP SENSOR(U403S-91) | DQA | Substantially Equivalent | Unimed Medical Supplies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 8, 2018. 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.