Data / Medical devices / United States / Bridges Consumer Healthcare
Bridges Consumer Healthcare: FDA-registered device maker in Chattanooga, TN, United States, 1 510(k) clearance
Bridges Consumer Healthcare is registered with the FDA (registration 3017591220) in Chattanooga, TN, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 12, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017591220
- Address
- 811 Broad Street Ste 600, Chattanooga, TN, United States, 37402
- Owner or operator
- Bridges Consumer Healthcare (10079008)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- November 14, 2020
- Registered through
- 2026
- Brand names listed
- Cystex UTI Test Strips, ThermaCare HeatWraps Joint Pain Therapy, ThermaCare HeatWraps Knee and Elbow, ThermaCare HeatWraps Lower Back and Hip, ThermaCare HeatWraps Menstrual, ThermaCare HeatWraps Muscle Pain Therapy, ThermaCare HeatWraps Neck, Wrist and Shoulder, 8-hour, ThermaCare HeatWraps Small Back
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Diazo (Colorimetric), Nitrite (Urinary, Non-Quant) | JMT | 1 | Complaint file establishment | accessdata.fda.gov |
| Pack, Hot Or Cold, Disposable | IMD | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Test, Urine Leukocyte | LJX | 1 | 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 |
|---|---|---|---|---|---|---|
| October 12, 2007 | K063295 | ACON UTI URINARY TRACT INFECTION TEST STRIPS | LJX | Substantially Equivalent | ACON Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
- All makers of Test, Urine Leukocyte
- All makers of Pack, Hot Or Cold, Disposable
Updated October 12, 2007. 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.