510(k) K022483

ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING by Johnson & Johnson Medical, Ltd. — Product Code FRO

K022483 is an FDA 510(k) premarket notification submitted by Johnson & Johnson Medical, Ltd. for the device "ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING". The FDA issued a decision of Substantially Equivalent on February 3, 2003. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Johnson & Johnson Medical, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 2003
Date Received
July 29, 2002
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