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FDA 510(k) Application Details - K242610
Device Classification Name
More FDA Info for this Device
510(K) Number
K242610
Device Name
8mm Monopolar Curved Scissors (470179)
Applicant
Iconocare Health
7825 East Redfield Rd.
Suite 103
Scottsdale, AZ 85260 US
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Contact
Rick Ferreira
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Regulation Number
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Classification Product Code
QSM
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More FDA Info for this Product Code
Date Received
09/03/2024
Decision Date
03/11/2025
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K242610
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