KMI OXY-BAN
Device Facts
| Record ID | K883848 |
|---|---|
| Device Name | KMI OXY-BAN |
| Applicant | Knight Medical, Inc. |
| Product Code | KPJ · General, Plastic Surgery |
| Decision Date | Mar 2, 1989 |
| Decision | SN |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.5650 |
| Device Class | Class 2 |
Regulatory Classification
Identification
A topical oxygen chamber for extremities is a device that is intended to surround a patient's limb and apply humidified oxygen topically at a pressure slightly greater than atmospheric pressure to aid healing of chronic skin ulcers such as bedsores.
Special Controls
*Classification.* Class II (special controls). The special control for this device is FDA's “Class II Special Controls Guidance: Topical Oxygen Chamber for Extremities.” See § 878.1(e) for the availability of this guidance document.
