Data / Medical devices / United States / Medical Accessories And Cables
Medical Accessories And Cables: FDA-registered device maker in Houston, TX, United States, 1 510(k) clearance
Medical Accessories And Cables is registered with the FDA (registration 3008963463) in Houston, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 10, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008963463
- Address
- 4669 Southwet FWY Suite #595, Houston, TX, United States, 77027
- Owner or operator
- medical accessories and cables (10036316)
- Roles
- Specification developer
- First device listed
- May 22, 2017
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable, Transducer And Electrode, Patient, (Including Connector) | DSA | 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 |
|---|---|---|---|---|---|---|
| October 10, 2008 | K082959 | PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS | DSA | Substantially Equivalent | Unimed Medical Supplies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 10, 2008. 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.