510(k) K061232

ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 by Acrymed, Inc. — Product Code FRO

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