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FDA 510(k) Application Details - K000297
Device Classification Name
Ligator, Hemorrhoidal
More FDA Info for this Device
510(K) Number
K000297
Device Name
Ligator, Hemorrhoidal
Applicant
ERCHINGER MEDIZINTECNIK
AMSTEL 320 I
AMSTERDAM 1017 AP NL
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Contact
DAGMAR MASER
Other 510(k) Applications for this Contact
Regulation Number
876.4400
More FDA Info for this Regulation Number
Classification Product Code
FHN
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/31/2000
Decision Date
04/24/2000
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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