510(k) K061232
K061232 is an FDA 510(k) premarket notification submitted by Acrymed, Inc. for the device "ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006". The FDA issued a decision of Substantially Equivalent on October 6, 2006. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Acrymed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 2006
- Date Received
- May 2, 2006
- 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