510(k) K070653
K070653 is an FDA 510(k) premarket notification submitted by Tyco Healthcare for the device "KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662". The FDA issued a decision of Substantially Equivalent on September 12, 2007. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Tyco Healthcare has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 12, 2007
- Date Received
- March 9, 2007
- 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