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FDA 510(k) Application Details - K152092
Device Classification Name
Electrode, Electrosurgical, Active, Urological
More FDA Info for this Device
510(K) Number
K152092
Device Name
Electrode, Electrosurgical, Active, Urological
Applicant
Olympus Winter & Ibe GmbH
Kuehnstrasse 61
Hamburg 22045 DE
Other 510(k) Applications for this Company
Contact
Katharina Schnackenburg
Other 510(k) Applications for this Contact
Regulation Number
876.4300
More FDA Info for this Regulation Number
Classification Product Code
FAS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/28/2015
Decision Date
10/26/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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