510(k) K032462
K032462 is an FDA 510(k) premarket notification submitted by Beiersdorf AG for the device "CURAD SILVER ACTIVE GEL BANDAGE". The FDA issued a decision of Substantially Equivalent on February 10, 2004. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Beiersdorf AG has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 2004
- Date Received
- August 11, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound, Drug
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type