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FDA 510(k) Application Details - K180327
Device Classification Name
Instrument, Biopsy
More FDA Info for this Device
510(K) Number
K180327
Device Name
Instrument, Biopsy
Applicant
Stryker Corporation
4100 E. Milham Avenue
Kalamazoo, MI 49001 US
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Contact
Kristi Ashton
Other 510(k) Applications for this Contact
Regulation Number
876.1075
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Classification Product Code
KNW
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More FDA Info for this Product Code
Date Received
02/06/2018
Decision Date
02/26/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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