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FDA 510(k) Application Details - K020269
Device Classification Name
Powder, Porcelain
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510(K) Number
K020269
Device Name
Powder, Porcelain
Applicant
PROCERA SANDVIK AB
LERKROGSVAGEN 19 VASTBERGA
STOCKHOLM S-12680 SE
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Contact
AGNETA ODEN
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Regulation Number
872.6660
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Classification Product Code
EIH
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More FDA Info for this Product Code
Date Received
01/28/2002
Decision Date
03/27/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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