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FDA 510(k) Application Details - K241809
Device Classification Name
Dressing, Wound, Drug
More FDA Info for this Device
510(K) Number
K241809
Device Name
Dressing, Wound, Drug
Applicant
Kane Biotech, Inc.
290-100 Innovation Drive
Winnipeg R3T 6G2 CA
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Contact
Lori Christofalos
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
FRO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/21/2024
Decision Date
07/19/2024
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K241809
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