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FDA 510(k) Application Details - K030559
Device Classification Name
Prosthesis, Esophageal
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510(K) Number
K030559
Device Name
Prosthesis, Esophageal
Applicant
RUSCH INTL.
50 PLANTATION DR.
JAFFERY, NH 03452 US
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Contact
KARENANN J BROZOWSKI
Other 510(k) Applications for this Contact
Regulation Number
878.3610
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Classification Product Code
ESW
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More FDA Info for this Product Code
Date Received
02/21/2003
Decision Date
06/30/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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