FDA 510(k) Application Details - K242610

Device Classification Name

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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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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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