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FDA 510(k) Application Details - K033593
Device Classification Name
Forceps, Biopsy, Electric, Reprocessed
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510(K) Number
K033593
Device Name
Forceps, Biopsy, Electric, Reprocessed
Applicant
CLEAR MEDICAL, INC.
1776 136TH PL. NE
BELLEVUE, WA 98005 US
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Contact
MIKE KOVACS
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Regulation Number
876.4300
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Classification Product Code
NLU
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More FDA Info for this Product Code
Date Received
11/13/2003
Decision Date
11/20/2003
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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