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FDA 510(k) Application Details - K001885
Device Classification Name
Urease, Photometric, Urea Nitrogen
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510(K) Number
K001885
Device Name
Urease, Photometric, Urea Nitrogen
Applicant
Ortho-Clinical Diagnostics, Inc.
100 INDIGO CREEK DR.
ROCHESTER, NY 14626-5101 US
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Contact
MARLENE SHULMAN
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Regulation Number
862.1770
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Classification Product Code
CDN
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More FDA Info for this Product Code
Date Received
06/21/2000
Decision Date
07/20/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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