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FDA 510(k) Application Details - K960231
Device Classification Name
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
More FDA Info for this Device
510(K) Number
K960231
Device Name
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Applicant
LIGHTHOUSE MEDICAL, INC.
100 BEAVER ST.
WALTHAM, MA 02154 US
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Contact
JENNA ANDELMAN
Other 510(k) Applications for this Contact
Regulation Number
876.4300
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Classification Product Code
KNS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/17/1996
Decision Date
07/31/1996
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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