510(k) K070333

ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL by Acrymed, Inc. — Product Code FRO

K070333 is an FDA 510(k) premarket notification submitted by Acrymed, Inc. for the device "ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL". The FDA issued a decision of Substantially Equivalent on July 10, 2007. 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
July 10, 2007
Date Received
February 5, 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