510(k) K082103
K082103 is an FDA 510(k) premarket notification submitted by Lifecell Corp. for the device "LTM WOUND DRESSING". The FDA issued a decision of Substantially Equivalent on October 8, 2008. The device falls under product code KGN (Wound Dressing With Animal-Derived Material(S)), a Class U device. Lifecell Corp. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 8, 2008
- Date Received
- July 25, 2008
- 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
- Regulation Number
- Review Panel
- SU
- Submission Type