510(k) K043063
K043063 is an FDA 510(k) premarket notification submitted by Oxyband Technologies, Inc. for the device "OXYBAND WOUND DRESSING". The FDA issued a decision of Substantially Equivalent on March 24, 2005. The device falls under product code NAD (Dressing, Wound, Occlusive), a Class I device regulated under 21 CFR 878.4020.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 24, 2005
- Date Received
- November 5, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound, Occlusive
- Device Class
- Class I
- Regulation Number
- 878.4020
- Review Panel
- SU
- Submission Type