510(k) K102942

CORELEADER ALGIPLASTER MODEL AP 050501 by Coreleader Biotech Co., Ltd. — Product Code FRO

K102942 is an FDA 510(k) premarket notification submitted by Coreleader Biotech Co., Ltd. for the device "CORELEADER ALGIPLASTER MODEL AP 050501". The FDA issued a decision of Substantially Equivalent on June 22, 2011. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Coreleader Biotech Co., Ltd. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 2011
Date Received
October 4, 2010
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