510(k) K173005
K173005 is an FDA 510(k) premarket notification submitted by Jiangsu Newvalue Medical Producst Co.,Ltd for the device "SURECELL Gelling Fiber Wound Dressing". The FDA issued a decision of Substantially Equivalent on May 25, 2018. The device falls under product code KGN (Wound Dressing With Animal-Derived Material(S)), a Class U device.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 25, 2018
- Date Received
- Sep 27, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wound Dressing With Animal-Derived Material(S)
- Device Class
- Class U
- Review Panel
- SU
- Submission Type
- 510(k)