510(k) K150557
K150557 is an FDA 510(k) premarket notification submitted by Podimetrics,Inc. for the device "Podimetrics Remote Temperature Monitoring System". The FDA issued a decision of Substantially Equivalent on October 8, 2015. The device falls under product code OIZ (Foot Examination Tool For Inflammatory Changes), a Class I device regulated under 21 CFR 890.5050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 8, 2015
- Date Received
- March 4, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Foot Examination Tool For Inflammatory Changes
- Device Class
- Class I
- Regulation Number
- 890.5050
- Review Panel
- HO
- Submission Type
Assist a patient to visualize the image and condition of the soles of their feet in connection with a daily self-examination for signs of inflammation on the sole of the foot. The device will assist the patient in determining when they should contact their healthcare provider for further diagnosis and treatment regarding any skin changes seen by a mirror and/or highlighted by the liquid crystal foot pads. Intended to be used as an adjunct to, and not in replacement of, periodic foot care and examinations conducted by a health care professional and used under the direction of a health care professional and does not diagnose any specific disease state.