510(k) K043296
K043296 is an FDA 510(k) premarket notification submitted by Covalontechnologies, Inc. for the device "COLACTIVE AG COLLAGEN WITH SILVER ANTIMICROBIAL DRESSING". The FDA issued a decision of Substantially Equivalent on June 6, 2005. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Covalontechnologies, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 2005
- Date Received
- November 29, 2004
- 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