510(k) K123892

MEPILEX TRANSFER AG by Molnlycke Health Care — Product Code FRO

K123892 is an FDA 510(k) premarket notification submitted by Molnlycke Health Care for the device "MEPILEX TRANSFER AG". The FDA issued a decision of Substantially Equivalent on April 5, 2013. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Molnlycke Health Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 2013
Date Received
December 18, 2012
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