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FDA 510(k) Application Details - K220124
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K220124
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
Pollogen Ltd.
6 Kaufman Street
Tel Aviv 6801298 IL
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Contact
Sharon Ravid
Other 510(k) Applications for this Contact
Regulation Number
878.4400
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Classification Product Code
GEI
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More FDA Info for this Product Code
Date Received
01/18/2022
Decision Date
02/17/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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